Tetrahydro-benzoazepine glycosidase inhibitors

ABSTRACT

Compounds of formula (I′), wherein A, R1, R2, T1, T2, T3, T4, L, W, Z, R′″, m and n have the meaning according to the claims, can be employed, inter alia, for the treatment of tauopathies and Alzheimer&#39;s disease.

The present invention relates to a compound of formula (I′) and amedicament comprising a compound of formula (I′)

and preferably a compound of formula (I)

wherein A, W, L, Z, R¹, R², R′″, T¹, T², T³, T⁴, m and n have themeaning according to the claims, and/or physiologically acceptablesalts, tautomers, solvates, stereoisomers and derivatives thereof. Thecompounds of formula (I′) or (I) can be used as glycosidase inhibitors.Objects of the invention are also pharmaceutical compositions comprisingthe compounds of formula (I′) or (I), and the use of the compounds offormula (I′) or (I) for the treatment of one or more tauopathies andAlzheimer's disease.

A wide range of cellular proteins, both nuclear and cytoplasmic, arepost-translationally modified by the addition of the monosaccharide2-acetamido-2-deoxy-β-D-glucopyranoside (p-N-acetyl glucosamine) whichis attached via an O-glycosidic linkage. This modification is generallyreferred to as O-linked N-acetylglucosamine or O-GlcNAc. The enzymeresponsible for post-translationally linking β-N-acetylglucosamine(GlcNAc) to specific serine and threonine residues of numerousnucleocytoplasmic proteins is O-GlcNAc transferase (OGTase). A secondenzyme, known as O-GlcNAcase, removes this post-translationalmodification to liberate proteins making the O-GlcNAc-modification adynamic cycle occurring several times during the lifetime of a protein.

O-GlcNAc-modified proteins regulate a wide range of vital cellularfunctions including, for example, transcription, proteasomal degradationand cellular signaling. O-GlcNAc is also found on many structuralproteins. For example, it has been found on a number of cytoskeletalproteins, including neurofilament proteins, synapsins, synapsin-specificclathrin assembly protein AP-3 and Ankyrin-G. O-GlcNAc modification hasbeen found to be abundant in the brain. It has also been found onproteins clearly implicated in the etiology of several diseasesincluding tauopathies, Alzheimer's disease (AD), synucleinopathies,Parkinson's disease, amyotrophic lateral sclerosis, and cancer.

For example, it is well established that AD and a number of relatedtauopathies including Down's Syndrome, progressive supranuclear palsy(PSP), Pick's disease, corticobasal degeneration (CBD), argyrophilicgrain disease (AGD), globular glial tauopathy (GGT), frontotemporaldementia and parkinsonism linked to chromosome-17 (FTLD-17, Niemann-PickType C disease are characterized, in part, by the development ofneurofibrillary tangles (NFTs). NFTs are also a histopathologicalhallmark of chronic traumatic encephalopathy that is a consequence oftraumatic brain injury. These NFTs are aggregates of paired helicalfilaments (PHFs) and are composed of an abnormal form of thecytoskeletal protein “tau”. Normally, tau stabilizes a key cellularnetwork of microtubules that is essential for distributing proteins andnutrients within neurons. In AD patients, however, tau becomeshyperphosphorylated, disrupting its normal function, forming PHFs andultimately aggregating to form NFTs. Six isoforms of tau are found inthe human brain. In AD patients, all six isoforms of tau are found inNFTs, and all are markedly hyperphosphorylated. Tau in healthy braintissue bears only 2 or 3 phosphate groups, whereas those found in thebrains of AD patients bear, on average, 8 phosphate groups. A clearparallel between NFT levels in the brains of AD patients and theseverity of dementia strongly supports a key role for tau dysfunction inAD. The precise causes of this hyperphosphorylation of tau remainelusive. Accordingly, considerable effort has been dedicated toward: a)elucidating the molecular physiological basis of tauhyperphosphorylation; and b) identifying strategies that could limit tauhyperphosphorylation in the hope that these might halt, or even reverse,the progression of tauopathies and Alzheimer's disease. Several lines ofevidence suggest that up-regulation of a number of kinases may beinvolved in hyperphosphorylation of tau, although very recently, analternative basis for this hyperphosphorylation has been advanced.

In particular, it has recently emerged that phosphate levels of tau areregulated by the levels of O-GlcNAc on tau. The presence of O-GlcNAc ontau has stimulated studies that correlate O-GlcNAc levels with tauphosphorylation levels. The recent interest in this field stems from theobservation that O-GlcNAc modification has been found to occur on manyproteins at amino acid residues that are also known to bephosphorylated. Consistent with this observation, it has been found thatincreases in phosphorylation levels result in decreased O-GlcNAc levelsand conversely, increased O-GlcNAc levels correlate with decreasedphosphorylation levels. This reciprocal relationship between O-GlcNAcand phosphorylation has been termed the “Yin-Yang hypothesis” and hasgained strong biochemical support by the recent discovery that theenzyme OGTase forms a functional complex with phosphatases that act toremove phosphate groups from proteins. Like phosphorylation, O-GlcNAc isa dynamic modification that can be removed and reinstalled several timesduring the lifespan of a protein. Suggestively, the gene encodingO-GlcNAcase has been mapped to a chromosomal locus that is linked to AD.Hyperphosphorylated tau in human AD brains has markedly lower levels ofO-GlcNAc than are found in healthy human brains. Very recently, it hasbeen shown that O-GlcNAc levels of soluble tau protein from human brainsaffected with AD are markedly lower than those from healthy brain.Furthermore, PHF from diseased brain was suggested to lack completelyany O-GlcNAc modification whatsoever. The molecular basis of thishypoglycosylation of tau is not known, although it may stem fromincreased activity of kinases and/or dysfunction of one of the enzymesinvolved in processing O-GlcNAc. Supporting this latter view, in bothPC-12 neuronal cells and in brain tissue sections from mice, anonselective N-acetylglucosaminidase inhibitor was used to increase tauO-GlcNAc levels, whereupon it was observed that phosphorylation levelsdecreased. Moreover, it has been described that the O-GlcNAcmodification of tau directly inhibits its aggregation without perturbingthe conformational properties of tau monomers. The implication of thesecollective results is that by maintaining healthy O-GlcNAc levels in ADpatients, such as by inhibiting the action of O-GlcNAcase (OGA), oneshould be able to block hyperphosphorylation of tau and all of theassociated effects of tau hyperphosphorylation, including the formationof NFTs and downstream effects. However, because the proper functioningof the lysosomal p-hexosaminidases is critical, any potentialtherapeutic intervention for the treatment of AD that blocks the actionof O-GlcNAcase would have to avoid the concomitant inhibition of bothlysosomal hexosaminidases A and B.

Consistent with the known properties of the hexosamine biosyntheticpathway, the enzymatic properties of O-GlcNAc transferase (OGTase), andthe reciprocal relationship between O-GlcNAc and phosphorylation, it hasbeen shown that decreased glucose availability in brain leads to tauhyperphosphorylation. The gradual impairment of glucose transport andmetabolism leads to decreased O-GlcNAc and hyperphosphorylation of tau(and other proteins). Accordingly, the inhibition of O-GlcNAcase shouldcompensate for the age-related impairment of glucose metabolism withinthe brains of health individuals as well as patients suffering from ADor related neurodegenerative diseases.

These results suggest that a malfunction in the mechanisms regulatingtau O-GlcNAc levels may be vitally important in the formation of NFTsand associated neurodegeneration. Good support for blocking tauhyperphosphorylation as a therapeutically useful intervention comes fromstudies showing that when transgenic mice harboring human tau aretreated with kinase inhibitors, they do not develop typical motordefects and, in another case, show a decreased level of insoluble tau.These studies provide a clear link between lowering tau phosphorylationlevels and alleviating AD-like behavioral symptoms in a murine model ofthis disease.

There is evidence indicating that the modification with O-GlcNAc mayhave a general function in preventing harmful protein aggregation. Thishas been directly demonstrated for the tau protein and also for theprotein alpha-synuclein that is a toxic aggregating protein associatedwith synucleinopathies, including Parkinson's disease. Two otheraggregating proteins that are associated with amyotrophic lateralysclerosis (Tar DNA binding protein-43 (TDP-43) and superoxide-dismutaseI (SOD-I)) and frontotemporal lobar degeneration (TDP-43) are known tocarry the O-GlcNAc modification. These results indicate that increasingO-GlcNAcylation with OGA inhibitors could be in general beneficial indiseases associated with protein aggregation.

There is also a large body of evidence indicating that increased levelsof O-GlcNAc protein modification provides protection against pathogeniceffects of stress in cardiac tissue, including stress caused byischemia, hemorrhage, hypervolemic shock, and calcium paradox. Forexample, activation of the hexosamine biosynthetic pathway (HBP) byadministration of glucosamine has been demonstrated to exert aprotective effect in animal models of ischemia/reperfusion, traumahemorrhage, hypervolemic shock and calcium paradox. Moreover, strongevidence indicates that these cardioprotective effects are mediated byelevated levels of protein O-GlcNAc modification. There is also evidencethat the O-GlcNAc modification plays a role in a variety ofneurodegenerative diseases, including Parkinson's disease and relatedsynucleinopathies, and Huntington's disease.

Humans have three genes encoding enzymes that cleave terminalβ-N-acetyl-glucosamine residues from glycoconjugates. The first of theseencodes the enzymeO-glycoprotein-2-acetamido-2-deoxy-β-D-glucopyranosidase (O-GlcNAcase).O-GlcNAcase is a member of family 84 of glycoside hydrolases.O-GlcNAcase acts to hydrolyze O-GlcNAc off of serine and threonineresidues of post-translationally modified proteins. Consistent with thepresence of O-GlcNAc on many intracellular proteins, the enzymeO-GlcNAcase appears to have a role in the etiology of several diseasesincluding type II diabetes, AD and cancer. Although O-GlcNAcase waslikely isolated earlier on, about 20 years elapsed before itsbiochemical role in acting to cleave O-GlcNAc from serine and threonineresidues of proteins was understood. More recently O-GlcNAcase has beencloned, partially characterized, and suggested to have additionalactivity as a histone acetyltransferase.

However, a major challenge in developing inhibitors for blocking thefunction of mammalian glycosidases, including O-GlcNAcase, is the largenumber of functionally related enzymes present in tissues of highereukaryotes. Accordingly, the use of non-selective inhibitors in studyingthe cellular and organismal physiological role of one particular enzymeis complicated because complex phenotypes arise from the concomitantinhibition of such functionally related enzymes. In the case ofβ-N-acetylglucosaminidases, existing compounds that act to blockO-GlcNAcase function are non-specific and act potently to inhibit thelysosomal p-hexosaminidases.

Low molecular weight OGA inhibitors are e.g. disclosed in theinternational applications WO 2008/025170 and WO 2014/032187, which arestructurally different from the compounds of the present invention.Further compounds that have some structurally similar elements aredisclosed in WO 2016/030443, U.S. Pat. Nos. 3,489,757, 3,299,067, WO99/21850, WO 2005/110982 and WO 2009/053373, WO 98/46590. However, thesecompounds do not show the improved pharmacological properties moreclosely described below.

Presently, no OGA inhibitor has reached the market. Thus, there is aneed for low molecular weight molecules that selectively inhibit OGA andprovide improved pharmacological properties that are of high relevancein drug development.

The present invention has the object of providing novel compounds havingvaluable properties, in particular those which can be used for thepreparation of medicaments.

In this regard, plasma protein binding (PPB) is an importantdifferentiating factor in drug development as it determines at least inpart the unbound, and thus, likely effective) drug concentrations atpharmacological target site. It is a well-acknowledged paradigm that, inthe absence of energy-dependent processes (e.g. transporter-mediatedactive organ uptake or efflux), once steady state equilibrium has beenreached, unbound drug concentration in plasma may be considered equal tounbound drug concentration in the target tissue(s), i.e. only theunbound drug in the tissues is available for binding to the targetreceptor and can therefore drive the desired pharmacologic activity(Free drug theory (FDT) (Bohnert, T. et al. J. Pharmaceutical Sciences2013, 102, 2953-2994). As a consequence, high plasma protein binding mayalso have a negative impact on efficacy since it is the free fraction ofdrug that is responsible for the pharmacological action.

Plasma protein binding information can be used to estimate the unboundand thus effective concentration of drugs in order to establishpharmacokinetic/pharmacodynamic (PKPD) relationships in animals andhumans. The extent of plasma protein binding across species providesimportant information for PKPD modelling and helps to better understandtranslational aspects and/or efficacy differences between animal modelsand humans.

In the present invention, the introduction of a sulfoximine groupresults in an increased unbound fraction (decreased PPB) for compoundsof Formula (I). In addition, the preferred compounds of the inventionprovide a low variability of fractions unbound across several animalspecies including humans. As a consequence, free drug concentrations intissues are increased, directly yielding higher unbound brainconcentrations (as measured by cerebrospinal fluid concentrations assurrogate) with similar effects measurable across different specieswhich often greatly improve predictability of human PK and result inlower effective human dose due to the same extent of increase of unboundfractions across species (Liu et al. J. Med. Chem. 2014, 57, 8238).

It has been surprisingly found that the compounds according to theinvention and salts thereof have very valuable pharmacologicalproperties. The compounds achieve increased metabolic stability, as e.g.shown in microsome stability assays.

Further, preferred glycosidase inhibitors of formula I provide increasedunbound, i.e. free fractions in plasma. Moreover, the preferredcompounds according to the invention and salts thereof consistentlyprovide increased free fractions in plasma across species includinghumans (low inter-species variability), which make them ideal forpharmaceutical development and their application as a drug.

The invention relates to compounds of formula (I′) or (I)

-   -   wherein    -   R¹, R² denote each independently a straight chain or branched        alkyl having 1 to 6 carbon atoms, wherein 1 to 5 hydrogen atoms        may be replaced by Hal or OH or one of R¹, R² denotes H, while        the other denotes a straight chain or branched alkyl having 1 to        6 carbon atoms, wherein 1 to 5 hydrogen atoms may be replaced by        Hal or OH or Rand R² may both denote H, if A denotes the        following group:

-   -   Z denotes H, OR³, OCF₃, Hal, a straight chain or branched alkyl        having 1 to 6 carbon atoms, wherein 1 to 5 hydrogen atoms may be        replaced by Hal or OR³    -   T¹, T², T³, T⁴ denote each independently CR′″ or N;    -   L is a single bond or one of the following groups: O, NR^(3′),        CH₂, OCH₂, CH₂CH₂, CONR^(3′), CONR^(3′)CH₂, NR^(3′)CO,        NR^(3′)COCH₂, SO₂NR^(3′), NR^(3′)SO₂, CONR^(3′)CH₂,        CH₂CONR^(3′), SO₂NR^(3′)CH₂, CH₂SO₂NR^(3′), CH₂NR^(3′)CO,        NR^(3′)SO₂CH₂, CH₂NR^(3′)SO₂, CH₂O, S(O)(NR^(3′)), N(SO)R^(3′),

-   -   m, n denote 0, 1 or 2, wherein m+n is 2;    -   A denotes one of the following groups:

-   -   X is N or CR′″;    -   X^(a) is N, NR³, C (in case it is an atom bearing a bond        connecting the group to the rest of the molecule) or CR′″;    -   X^(b) is N or C;    -   Y is O, S, SO or SO₂;    -   R′, R″ denote each independently H, Hal or straight chain or        branched alkyl having 1 to 12 carbon atoms;    -   R′″, R independently denote H, Hal, NR³R⁴, CHR³R⁴, OR³, CN or a        straight chain or branched alkyl having 1 to 12 carbon atoms,        wherein 1 to 3 CH₂-groups may be replaced by a group selected        from O, NR³, S, SO, SO₂, S(O)(NR^(3′)), N(SO)R³, CO, COO, OCO,        CONR³, NR³CO,

-   -   -   and wherein 1 to 5 hydrogen atoms may be replaced by Hal,            NR³R⁴ or NO₂ or by one of the following groups:

-   -   -   or R′″, R″″ independently denote one of the following            groups:

-   -   R³, R⁴ denote each independently H or a straight chain or        branched alkyl group having 1 to 12 carbon atoms;    -   R^(3a) denotes a straight chain or branched alkyl group having 1        to 12 carbon atoms;    -   W denotes Q or R    -   Q denotes one of the following groups:

-   -   Z¹ is S, O, NR³;    -   Z², Z³ independently denote CR⁵, CR⁶ or N;    -   Z⁴ is N, CH, CON, COCH;    -   Z⁵ is O, NR⁸, CHR⁵, SO₂, S(O)(NR^(3′)), N(SO)R^(3′),

-   -   Z⁶ is CH₂, CO, S(O)(NR^(3′)), N(SO)R^(3′),

-   -   Z⁷ is C(R^(3′))₂, S, O, NR^(3′);    -   s denotes 0 or 1;    -   T is N, CH or CR¹;    -   R^(3′) denotes H or a straight chain or branched alkyl group        having 1 to 12 carbon atoms, wherein 1 to 3 CH₂-groups may be        replaced by a group selected from SO₂, CO, O and wherein 1 to 5        hydrogen atoms may be replaced by Hal;    -   R, R⁵, R⁶, R⁷ independently denote H, Hal, CN, OH, NR³R⁴, NO₂ or        a straight chain or branched alkyl having 1 to 12 carbon atoms,        wherein 1 to 3 CH₂-groups may be replaced by a group selected        from O, NR³, S, SO, SO₂, S(O)(NR^(3′)), N(SO)R³, CO, COO, OCO,        CONR³, NR³CO

-   -   -   and wherein 1 to 5 hydrogen atoms may be replaced by Hal,            NR³R⁴, NO₂, OR³, Het, Ar, Cyc or by one of the following            groups:

-   -   -   or R, R⁵, R⁶, R⁷ denote Ar, Het or Cyc or one of the            following groups:

-   -   R⁸ denotes H or straight chain or branched alkyl having 1 to 12        carbon atoms, wherein 1 to 3 CH₂-groups may be replaced by a        group selected from SO, SO₂, S(O)(NR^(3′)), N(SO)R^(3′), CO,        COO, OCO, CONR³, NR³CO, and

-   -   -   and further wherein 1 to 5 hydrogen atoms may be replaced by            CN, OR³, SR³, Hal, NR³R⁴, NO₂ or by one of the following            groups:

-   -   -   or R⁸ denote one of the following groups:

-   -   Hal denotes F, Cl, Br or I;    -   Het denotes a saturated, unsaturated or aromatic ring, being        monocyclic or bicyclic or fused-bicyclic and having 3- to        8-members and containing 1 to 4 heteroatoms selected from N, O        and S, which may be substituted by 1 to 3 substituents selected        from R⁵, Hal and OR³;    -   Ar denotes a 6-membered carbocyclic aromatic ring or a fused or        non-fused bicylic aromatic ring system, which is optionally        substituted by 1 to 3 substituents independently selected from        R⁵, OR³ and Hal;    -   Cyc denotes a saturated or an unsaturated carbocyclic ring        having from 3 to 8 carbon atoms which is optionally substituted        by 1 to 3 substituents independently selected from R⁵, Hal and        OH;    -   t and q denote independently from one another 0, 1, 2 or 3, with        t+q≥1,        and pharmaceutically usable derivatives, solvates, salts,        prodrugs, tautomers, enantiomers, racemates and stereoisomers        thereof, including mixtures thereof in all ratios and compounds        of formula I, wherein one or more H atoms may be replaced by D        (deuterium).

In a preferred embodiment, the present invention relates to a compoundof formula (I)

-   -   wherein    -   R¹, R² denote each independently H or a straight chain or        branched alkyl having 1 to 6 carbon atoms, wherein 1 to 5        hydrogen atoms may be replaced by Hal or OH;    -   T¹, T², T³, T⁴ denote each independently CR′″ or N;    -   L is a single bond or one of the following groups: O, NR^(3′),        CH₂, OCH₂, CH₂CH₂, CONR^(3′), CONR^(3′)CH₂, NR^(3′)CO,        NR^(3′)COCH₂, SO₂NR^(3′), NR³'SO₂, CONR^(3′)CH₂, CH₂CONR^(3′),        SO₂NR^(3′)CH₂, CH₂SO₂NR³, CH₂NR^(3′)CO, NR^(3′)SO₂CH₂,        CH₂NR^(3′)SO₂, CH₂O, S(O)(NR^(3′)), N(SO)R^(3′),

-   -   m, n denote 0, 1 or 2, wherein m+n is 2;    -   A denotes one of the following groups:

-   -   X is N or CR′″;    -   X^(a) is N, NR 3, C or CR′″;    -   X^(b) is N or C;    -   Y is O, S, SO or SO₂;    -   R′, R″ denote each independently H, Hal or straight chain or        branched alkyl having 1 to 12 carbon atoms; R′″, R″″        independently denote H, Hal, NR³R⁴, CHR³R⁴, OR³, CN or a        straight chain or branched alkyl having 1 to 12 carbon atoms,        wherein 1 to 3 CH₂-groups may be replaced by a group selected        from O, NR³, S, SO, SO₂, S(O)(NR^(3′)), N(SO)R^(3′), CO, COO,        OCO, CONR³, NR³CO,

-   -   -   and wherein 1 to 5 hydrogen atoms may be replaced by Hal,            NR³R⁴ or NO₂ or by one of the following groups:

-   -   -   or R′″, R″″ independently denote one of the following            groups:

-   -   R³, R⁴ denote each independently H or a straight chain or        branched alkyl group having 1 to 12 carbon atoms;    -   R^(3a) denote a straight chain or branched alkyl group having 1        to 12 carbon atoms;    -   W denotes Q or R    -   Q denotes one of the following groups:

-   -   Z¹ is S, O, NR³;    -   Z², Z³ independently denote CR⁵, CR⁶ or N;    -   Z⁴ is N, CH, CON, COCH;    -   Z⁵ is O, NR⁸, CHR⁵, SO₂, S(O)(NR^(3′)), N(SO)R^(3′),

-   -   Z⁶ is CH₂, CO, S(O)(NR^(3′)), N(SO)R^(3′),

-   -   Z⁷ is C(R^(3′))₂, S, O, NR^(3′);    -   s denotes 0 or 1;    -   T is N, CH or CR⁷;    -   R^(3′) denotes H or a straight chain or branched alkyl group        having 1 to 12 carbon atoms, wherein 1 to 3 CH₂-groups may be        replaced by a group selected from SO₂, CO, 0 and wherein 1 to 5        hydrogen atoms may be replaced by Hal;    -   R, R⁵, R⁶, R⁷ independently denote H, Hal, CN, OH, NR³R⁴, NO₂ or        a straight chain or branched alkyl having 1 to 12 carbon atoms,        wherein 1 to 3 CH₂-groups may be replaced by a group selected        from O, NR³, S, SO, SO₂, S(O)(NR^(3′)), N(SO)R³, CO, COO, OCO,        CONR³, NR³CO

-   -   -   and wherein 1 to 5 hydrogen atoms may be replaced by Hal,            NR³R⁴, NO₂, OR³, Het, Ar, Cyc or by one of the following            groups:

-   -   -   or R, R⁵, R⁶, R⁷ denote Ar, Het or Cyc or one of the            following groups:

-   -   R⁸ denotes H or straight chain or branched alkyl having 1 to 12        carbon atoms, wherein 1 to 3 CH₂-groups may be replaced by a        group selected from SO, SO₂, S(O)(NR^(3′)), N(SO)R^(3′), CO,        COO, OCO, CONR³, NR³CO, and

-   -   -   and further wherein 1 to 5 hydrogen atoms may be replaced by            CN, OR³, SR³, Hal, NR³R⁴, NO₂ or by one of the following            groups:

-   -   -   or R⁸ denote one of the following groups:

-   -   Hal denotes F, Cl, Br or I;    -   Het denotes a saturated, unsaturated or aromatic ring, being        monocyclic or bicyclic or fusedbicyclic and having 3 to 8        members and containing 1 to 4 heteroatoms selected from N, O and        S, which may be substituted by 1 to 3 substituents selected from        R⁵, Hal and OR³;    -   Ar denotes a 6-membered carbocyclic aromatic ring or a fused or        non-fused bicylic aromatic ring system, which is optionally        substituted by 1 to 3 substituents independently selected from        R⁵, OR³ and Hal;    -   Cyc denotes a saturated or an unsaturated carbocyclic ring        having from 3 to 8 carbon atoms which is optionally substituted        by 1 to 3 substituents independently selected from R⁵, Hal and        OH;    -   t and q denote independently from one another 0, 1, 2 or 3, with        t+q≥1,        and pharmaceutically usable derivatives, solvates, salts,        prodrugs, tautomers, enantiomers, racemates and stereoisomers        thereof, including mixtures thereof in all ratios and compounds        of formula I, wherein one or more H atoms may be replaced by D        (deuterium) with the proviso that the following compounds are        excluded:

Specifically, formula (I′) includes the following preferred compounds offormulae Ia′, Ib′, Ic′, Id′, Ie′, If′, Ig′ and Ih′:

-   -   wherein A, W, Z, L, T¹, T², T³, T⁴, R′″, m and n have the        meaning given above and preferably, wherein R¹ and R² denote        each independently a straight chain or branched alkyl having 1        to 6 carbon atoms, wherein 1 to 5 hydrogen atoms may be replaced        by Hal or OH.

Specifically, formula (I) includes the following preferred compounds offormulae Ia″, Ib″, Ic″, Id″, Ie″, If″, Ig″ and Ih″:

-   -   wherein Z is OH and wherein A, W, L, T¹, T², T³, T⁴, R′″, m and        n have the meaning given above and preferably, wherein R¹ and R²        denote each independently a straight chain or branched alkyl        having 1 to 6 carbon atoms, wherein 1 to 5 hydrogen atoms may be        replaced by Hal or OH.

Specifically, formula (I′) includes the following preferred compounds offormulae Ia′″, Ib′″, Ic′″, Id′″, Ie′″, If′″, Ig′″ and Ih′″:

-   -   wherein Z is F and wherein A, W, L, T¹, T², T³, T⁴, R′″, m and n        have the meaning given above and preferably, wherein R¹ and R²        denote each independently a straight chain or branched alkyl        having 1 to 6 carbon atoms, wherein 1 to 5 hydrogen atoms may be        replaced by Hal or OH.

Specifically, formula (I) includes the following most preferredcompounds of formulae Ia, Ib, Ic, Id, Ie, If, Ig and Ih:

-   -   wherein A, W, L, T¹, T², T³, T⁴, R′″, m and n have the meaning        given above and preferably, wherein R¹ and R² denote each        independently a straight chain or branched alkyl having 1 to 6        carbon atoms, wherein 1 to 5 hydrogen atoms may be replaced by        Hal or OH.

Compounds of formula I′ of the following group are especially preferred:

wherein A, W, Z, L, R¹, R², R′″, T¹, T², m and n have the meaning givenabove

Compounds of formula I′ of the following group are especially preferred:

Wherein Z is OH and wherein A, W, L, R¹, R², R′″, T¹, T², m and n havethe meaning given above

Compounds of formula I′ of the following group are especially preferred:

wherein Z is F and wherein A, W, L, R¹, R², R′″, T¹, T², m and n havethe meaning given above

Compounds of formula I of the following group are especially preferred:

wherein A, W, L, R¹, R², R′″, T¹, T², m and n have the meaning givenabove

Compounds of formula Ig′, Ih′, Ig and Ih are especially preferred if Adenotes

The invention also relates to a composition or mixture comprisingcompounds of formulae Ia′ and Ic′ or a mixture comprising compounds offormulae Ib′ and Id′ or a mixture comprising compounds of formulae Ie′or If′ or a mixture comprising compounds of formulae Ig′ and Ih′, havingidentical groups A, W, Z, L, R¹, R², T¹, T², T³, T⁴, R′″, m and n, inequal or unequal amounts.

The invention also relates to a composition or mixture comprisingcompounds of formulae Ia and Ic or a mixture comprising compounds offormulae Ib and Id or a mixture comprising compounds of formulae Ie orIf or a mixture comprising compounds of formulae Ig and Ih, havingidentical groups A, W, L, R¹, R², T¹, T², T³, T⁴, R′″, m and n, in equalor unequal amounts.

Preferably, the definition of R¹ is selected from methyl and ethyl, andis most preferably methyl.

Preferably, the definition of R² is selected from H, methyl and ethyl,and most preferably from H and methyl. More preferably, R¹ is methyl,while R² denotes H.

More preferably, if the group A is other than

the definition of R¹ is preferably selected from methyl, while R² ispreferably selected from H, methyl and ethyl, and most preferably from Hand methyl.

In a further preferred embodiment, if the group A is

the definition of R² is selected from methyl and ethyl, and is mostpreferably methyl. In this case, more preferably R¹ denotes H.

In preferred embodiments of the invention, the group

more specifically denotes one of the following groups:

Moreover, compounds of formula Ii′

wherein A denotes

Moreover, compounds of formula Ii″

wherein Z denotes OH and A denotes

Moreover, compounds of formula Ii′″

wherein Z denotes F and A denotes

Moreover, compounds of formula Ii

wherein A denotes

Compounds of formula I are preferred, wherein m and n simultaneouslydenote 1.

Compounds of formula I are preferred, wherein L is a single bond or —O—.

Compounds of formula I are preferred, wherein T¹, T², T³ and T⁴ denoteCH or one or two of T¹, T², T³ and T⁴ denote N.

In further preferred embodiments, compounds of formula I bear an N-oxidegroup in the tetrahydro-benzoazepine moiety at the position of thetertiary N-atom of the saturated ring.

In the following and above, a reference to compounds of formula Iincludes all sub-formulae, such as formula Ia and Ib, if not indicatedotherwise or a if no different meaning is intended in view of thecontext.

If individual groups and indices, such as T or X, occur more than oncein a compound of formula I, they can have the same or different meaningsaccording to the respective definition of that group.

A further preferred compound of formula I is a single enantiopure orenantiomerically enriched isomer, i.e. a compound wherein thestereogenic center bearing the group R¹ has an S-configuration and anyother stereogenic center, if present within the compound, has either anS- or an R-configuration.

Preferred compounds of the present invention are preferably used assingle isomer in their non-racemic form, i.e. as diasteromerically andenatiomerically pure compounds or their diastereomerically andenaniomerically enriched mixtures of the respective diastereomers andenantiomers.

In general, compounds of formula I are preferred that contain one oremore preferred groups such as T and indices such as n. Compounds offormula I are the more preferred, the more preferred groups or indicesthey contain.

If substituents, such as the group R⁸, are connected to the remainder ofthe molecule through a heteroatom, the connecting atom in the respectivegroup is preferably a carbon atom or the respective group is H.

The invention also relates to the use of compounds of formula (I′) or(I) as a medicament.

In the meaning of the present invention, the compound is defined toinclude pharmaceutically usable derivatives, solvates, prodrugs,tautomers, enantiomers, racemates and stereoisomers thereof, includingmixtures thereof in all ratios.

The term “pharmaceutically usable derivatives” is taken to mean, forexample, the salts of the compounds according to the invention and alsoso-called prodrug compounds. The term “solvates” of the compounds istaken to mean adductions of inert solvent molecules onto the compounds,which are formed owing to their mutual attractive force. Solvates are,for example, mono- or dihydrates or alkoxides. The invention alsocomprises solvates of salts of the compounds according to the invention.The term “prodrug” is taken to mean compounds according to the inventionwhich have been modified by means of, for example, alkyl or acyl groups,sugars or oligopeptides and which are rapidly cleaved in the organism toform the effective compounds according to the invention. These alsoinclude biodegradable polymer derivatives of the compounds according tothe invention. It is likewise possible for the compounds of theinvention to be in the form of any desired prodrugs such as, forexample, esters, carbonates, carbamates, ureas, amides or phosphates, inwhich cases the actually biologically active form is released onlythrough metabolism. Any compound that can be converted in-vivo toprovide the bioactive agent (i.e. compounds of the invention) is aprodrug within the scope and spirit of the invention. Various forms ofprodrugs are well known in the art. It is further known that chemicalsubstances are converted in the body into metabolites which may whereappropriate likewise elicit the desired biological effect—in somecircumstances even in more pronounced form. Any biologically activecompound that was converted in-vivo by metabolism from any of thecompounds of the invention is a metabolite within the scope and spiritof the invention.

The compounds of the invention may be present in the form of theirdouble bond isomers as pure E or Z isomers, or in the form of mixturesof these double bond isomers. Where possible, the compounds of theinvention may be in the form of the tautomers, such as keto-enoltautomers. All stereoisomers of the compounds of the invention arecontemplated, either in a mixture or in pure or substantially pure form.The compounds of the invention can have asymmetric centers at any of thecarbon atoms. Consequently, they can exist in the form of theirracemates, in the form of the pure enantiomers and/or diastereomers orin the form of mixtures of these enantiomers and/or diastereomers. Themixtures may have any desired mixing ratio of the stereoisomers. Thus,for example, the compounds of the invention which have one or morecenters of chirality and which occur as racemates or as diastereomermixtures can be fractionated by methods known per se into their opticalpure isomers, i.e. enantiomers or diastereomers. The separation of thecompounds of the invention can take place by column separation on chiralor non-chiral phases or by re-crystallization from an optionallyoptically active solvent or with use of an optically active acid or baseor by derivatization with an optically active reagent such as, forexample, an optically active alcohol, and subsequent elimination of theradical.

The invention also relates to the use of mixtures of the compoundsaccording to the invention, for example mixtures of two diastereomers,for example in the ratio 1:1, 1:2, 1:3, 1:4, 1:5, 1:10, 1:100 or 1:1000.These are particularly preferably mixtures of stereoisomeris.

An enantiomerically enriched mixture denotes a compound of Formula (I′)or (I) or related formula having an enantiomeric excess, as measured bymethods well known by one skilled in the art, of 10% or more, preferably50% or more, and more preferably more than 95%. Most preferably anenantiomerically enriched mixture denotes a compound of Formula (I′) or(I) or related Formulae having an enantiomeric excess of more than 98%.

The nomenclature as used herein for defining compounds, especially thecompounds according to the invention, is in general based on the rulesof the IUPAC-organization for chemical compounds and especially organiccompounds. The compounds of invention have been named according to thestandards used in the program AutoNom 2000 or ACD Lab Version 12.01 orInstant JChem Version: 15.12.7.0. The determination of thestereochemistry (S) or (R) is performed using standard rules of thenomenclature well known by one skilled in the art.

The term “unsubstituted” means that the corresponding radical, group ormoiety has no substituents. The term “substituted” means that thecorresponding radical, group or moiety has one or more substituents.Where a radical has a plurality of substituents, and a selection ofvarious substituents is specified, the substituents are selectedindependently of one another and do not need to be identical. Eventhough a radical has a plurality of a specific-designated substituentthe expression of such substituent may differ from each other (e.g.methyl and ethyl). It shall be understood accordingly that a multiplesubstitution by any radical of the invention may involve identical ordifferent radicals. Hence, if individual radicals occur several timeswithin a compound, the radicals can adopt any of the meanings indicated,independently of one another.

The term “alkyl” or “alkyl group” refers to acyclic saturated orunsaturated hydrocarbon radicals, which may be branched orstraight-chain and preferably have 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10carbon atoms, i.e. C₁-C₁₀-alkanyls. Examples of suitable alkyl radicalsare methyl, ethyl, n-propyl, isopropyl, 1,1-, 1,2- or2,2-dimethylpropyl, 1-ethylpropyl, 1-ethyl-1-methylpropyl,1-ethyl-2-methylpropyl, 1,1,2- or 1,2,2-trimethylpropyl, n-butyl,isobutyl, sec-butyl, tert-butyl, 1-, 2- or 3-methylbutyl, 1,1-, 1,2-,1,3-, 2,2-, 2,3- or 3,3-dimethylbutyl, 1- or 2-ethylbutyl, n-pentyl,iso-pentyl, neo-pentyl, tert-pentyl, 1-, 2-, 3- or -methyl-pentyl,n-hexyl, 2-hexyl, isohexyl, n-heptyl, n-octyl, n-nonyl, n-decyl,n-undecyl, n-dodecyl, n-tetradecyl, n-hexadecyl, n-octadecyl,n-icosanyl, n-docosanyl. In certain embodiments of the invention, 1 ormore, preferable 1 to 3 CH₂ groups may be replaced by other divalentgroups according to the definitions given above and below. In aparticular embodiment, an H atom of alkyl may be replaced by Cyc.

In an embodiment of the invention, alkyl denotes unbranched or branchedalkyl having 1-10 C atoms, in which 1-7 H atoms may be replacedindependently from one another by Hal. A preferred embodiment of alkyldenotes unbranched or branched alkyl having 1-6 C atoms, in which 1-4atoms may be replaced independently from one another by Hal. In a morepreferred embodiment of the invention, alkyl denotes unbranched orbranched alkyl having 1-4 C atoms, in which 1-3 H atoms can be replacedindependently from one another by Hal, particularly by F and/or Cl. Itis most preferred that alkly denotes unbranched or branched alkyl having1-6 C atoms. Highly preferred is C₁₋₄-alkyl. A C₁₋₄-alkyl radical is forexample a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl,sec-butyl, tert-butyl, fluoromethyl, difluoromethyl, trifluoromethyl,pentafluoroethyl, 1,1,1-trifluoroethyl or bromomethyl, especiallymethyl, ethyl, propyl or trifluoromethyl. It shall be understood thatthe respective denotation of alkyl is independently of one another inany radical of the invention.

The terms “cycloalkyl” or “Cyc” for the purposes of this inventionrefers to saturated and partially unsaturated non-aromatic cyclichydrocarbon groups/radicals, having 1 to 3 rings, that contain 3 to 20,preferably 3 to 12, more preferably 3 to 9 carbon atoms. The cycloalkylradical may also be part of a bi- or polycyclic system, where, forexample, the cycloalkyl radical is fused to an aryl, heteroaryl orheterocyclyl radical as defined herein by any possible and desired ringmember(s). The bonding to the compounds of the general formula (I′) or(I) can be effected via any possible ring member of the cycloalkylradical. Examples of suitable cycloalkyl radicals are cyclopropyl,cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl,cyclodecyl, cyclohexenyl, cyclopentenyl and cyclooctadienyl.

In an embodiment of the invention, Cyc denotes cycloalkyl having 3-7 Catoms, in which 1-4 H atoms may be replaced independently of one anotherby Hal. Preferred is C₃-C₇-cycloalkyl. More preferred isC₄-C₇-cycloalkyl. Most preferred is C₅-C₇-cycloalkyl, i.e. cyclopentyl,cyclohexyl or cycloheptyl, highly preferably cyclohexyl. It shall beunderstood that the respective denotation of Cyc is independently of oneanother in any radical of the invention.

The term “Ar”, “aryl” or “carboaryl” for the purposes of this inventionrefers to a mono- or polycyclic aromatic hydrocarbon systems having 3 to14, preferably 3-12, more preferably 4 to 12, most preferably 5 to 10,highly preferably 6 to 8 carbon atoms, which can be optionallysubstituted. The term “Ar” or “aryl” also includes systems in which thearomatic cycle is part of a bi- or polycyclic saturated, partiallyunsaturated and/or aromatic system, such as where the aromatic cycle isfused to an aryl, cycloalkyl, heteroaryl or heterocyclyl group asdefined herein via any desired and possible ring member of the arylradical. The bonding to the compounds of the general formula (I′) or (I)can be effected via any possible ring member of the aryl radical.Examples of suited aryl radicals are phenyl, biphenyl, naphthyl,1-naphthyl, 2-naphthyl and anthracenyl, but likewise indanyl, indenyl or1,2,3,4-tetrahydronaphthyl. Preferred carboaryls of the invention areoptionally substituted phenyl, naphthyl and biphenyl, more preferablyoptionally substituted monocylic carboaryl having 6-8 C atoms, mostpreferably optionally substituted phenyl.

Ar and aryl are preferably selected from the following group: phenyl,o-, m- or p-tolyl, o-, m- or p-ethylphenyl, o-, m- or p-propylphenyl,o-, m- or p-isopropylphenyl, o-, m- or p-tert.-butylphenyl, o-, m- orp-hydroxyphenyl, o-, m- or p-methoxyphenyl, o-, m- or p-ethoxyphenyl,o-, m- or p-fluoro-phenyl, o-, m- or p-bromophenyl, o-, m- orp-chlorophenyl, o-, m- or p-sulfonamidophenyl, o-, m- orp-(N-methyl-sulfonamido)phenyl, o-, m- orp-(N,N-dimethyl-sulfonamido)-phenyl, o-, m- orp-(N-ethyl-N-methyl-sulfonamido)phenyl, o-, m- orp-(N,N-diethyl-sulfonamido)-phenyl, particularly 2,3-, 2,4-, 2,5-, 2,6-,3,4- or 3,5-difluorophenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or3,5-dichlorophenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5-dibromophenyl,2,3,4-, 2,3,5-, 2,3,6-, 2,4,6- or 3,4,5-trichlorophenyl,2,4,6-trimethoxyphenyl, 2-hydroxy-3,5-dichlorophenyl, p-iodophenyl,4-fluoro-3-chlorophenyl, 2-fluoro-4-bromophenyl,2,5-difluoro-4-bromophenyl, 3-bromo-6-methoxyphenyl,3-chloro-6-methoxyphenyl or 2,5-dimethyl-4-chlorophenyl.

Irrespective of further substitutions, Het denotes preferably 2- or3-furyl, 2- or 3-thienyl, 1-, 2- or 3-pyrrolyl, 1-, 2, 4- or5-imidazolyl, 1-, 3-, 4- or 5-pyrazolyl, 2-, 4- or 5-oxazolyl, 3-, 4- or5-isoxazolyl, 2-, 4- or 5-thiazolyl, 3-, 4- or 5-isothiazolyl, 2-, 3- or4-pyridyl, 2-, 4-, 5- or 6-pyrimidinyl, furthermore preferably1,2,3-triazoM-, -4- or -5-yl, 1,2,4-triazo-, -3- or 5-yl, 1- or5-tetrazolyl, 1,2,3-oxadiazol-4- or -5-yl, 1,2,4-oxadiazol-3- or -5-yl,1,3,4-thiadiazol-2- or -5-yl, 1,2,4-thiadiazol-3- or -5-yl,1,2,3-thiadiazol-4- or -5-yl, 3- or 4-pyridazinyl, pyrazinyl, 1-, 2-,3-, 4-, 5-, 6- or 7-indolyl, 4- or 5-iso-5i-ndolyl, indazolyl, 1-, 2-,4- or 5-benzimidazolyl, 1-, 3-, 4-, 5-, 6- or 7-benzo-pyrazolyl, 2-, 4-,5-, 6- or 7-benzoxazolyl, 3-, 4-, 5-, 6- or 7-benzisoxazolyl, 2-, 4-,5-, 6- or 7-benzothiazolyl, 2-, 4-, 5-, 6- or 7-benzisothiazolyl, 4-,5-, 6- or 7-benz-2,1,3-oxadiazolyl, 2-, 3-, 4-, 5-, 6-, 7- or8-quinolyl, 1-, 3-, 4-, 5-, 6-, 7- or 8-isoquinolyl, 3-, 4-, 5-, 6-, 7-or 8-cinnolinyl, 2-, 4-, 5-, 6-, 7- or 8-quinazolinyl, 5- or6-quinoxalinyl, 2-, 3-, 5-, 6-, 7- or 8-2H-benzo-1,4-oxazinyl, furtherpreferably 1,3-benzodioxol-5-yl, 1,4-benzodioxan-6-yl,2,1,3-benzothiadiazol-4-, -5-yl or 2,1,3-benzoxadiazol-5-yl,azabicyclo-[3.2.1]octyl or dibenzofuranyl.

The heterocyclic radicals may also be partially or fully hydrogenated.

Irrespective of further substitutions, Het can thus also denote,preferably, 2,3-dihydro-2-, -3-, -4- or -5-furyl, 2,5-dihydro-2-, -3-,-4- or 5-furyl, tetra-hydro-2- or -3-furyl, 1,3-dioxolan-4-yl,tetrahydro-2- or -3-thienyl, 2,3-di-hydro-1-, -2-, -3-, -4- or-5-pyrrolyl, 2,5-dihydro-1-, -2-, -3-, -4- or -5-pyrrolyl, 1-, 2- or3-pyrrolidinyl, tetrahydro-1-, -2- or -4-imidazolyl, 2,3-dihydro-1-,-2-, -3-, -4- or -5-pyrazolyl, tetrahydro-1-, -3- or -4-pyrazolyl,1,4-dihydro-1-, -2-, -3- or -4-pyridyl, 1,2,3,4-tetrahydro-1-, -2-, -3-,-4-, -5- or -6-pyridyl, 1-, 2-, 3- or 4-piperidinyl, 2-, 3- or4-morpholinyl, tetrahydro-2-, -3- or -4-pyranyl, 1,4-dioxanyl,1,3-dioxan-2-, -4- or -5-yl, hexahydro-1-, -3- or -4-pyridazinyl,hexahydro-1-, -2-, -4- or -5-pyrimidinyl, 1-, 2- or 3-piperazinyl,1,2,3,4-tetrahydro-1-(-2-, -3-, -4-, -5-, -6-, -7- or -8-quinolyl,1,2,3,4-tetra-hydro-1-,-2-,-3-, -4-, -5-, -6-, -7- or -8-isoquinolyl,2-, 3-, 5-, 6-, 7- or 8-3,4-dihydro-2H-benzo-1,4-oxazinyl, furthermorepreferably 2,3-methylene-dioxyphenyl, 3,4-methylenedioxyphenyl,2,3-ethylenedioxyphenyl, 3,4-ethylenedioxyphenyl,3,4-(difluoromethylenedioxy)phenyl, 2,3-dihydro-benzofuran-5- or 6-yl,2,3-(2-oxomethylenedioxy)phenyl or also3,4-di-hydro-2H-1,5-benzodioxepin-6- or -7-yl, furthermore preferably2,3-dihydrobenzofuranyl, 2,3-dihydro-2-oxofuranyl, 3,4-dihydro-2-oxo-1H-quinazolinyl, 2,3-dihydrobenzoxazolyl, 2-oxo-2,3-dihydrobenzoxazolyl,2,3-dihydrobenzimidazolyl, 1,3-dihydroindole, 2-oxo-1,3-dihydroindole or2-oxo-2, 3-dihydrobenzimidazolyl.

Het preferably denotes piperidinyl, 4-hydroxypiperidinyl, piperazinyl,4-methylpiperazinyl, pyrrolidinyl, morpholinyl, dihydro-pyrazolyl,dihydro-pyridyl, dihydropyranyl, furyl, thienyl, pyrrolyl, imidazolyl,pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyridyl,pyrimidinyl, triazolyl, tetrazolyl, oxadiazolyl, thiadiazolyl,pyridazinyl, pyrazinyl, quinolyl, isoquinolyl, benzimidazolyl,benzotriazolyl, indolyl, benzo-1,3-dioxolyl,2,3-dihydro-benzo[1,4]dioxinyl, indazolyl or benzothiadiazolyl, each ofwhich is unsubstituted or mono-, di- or trisubstituted.

The term “halogen”, “halogen atom”, “halogen substituent” or “Hal” forthe purposes of this invention refers to one or, where appropriate, aplurality of fluorine (F, fluoro), bromine (Br, bromo), chlorine (Cl,chloro) or iodine (I, iodo) atoms. The designations “dihalogen”,“trihalogen” and “perhalogen” refer respectively to two, three and foursubstituents, where each substituent can be selected independently fromthe group consisting of fluorine, chlorine, bromine and iodine. Halogenpreferably means a fluorine, chlorine or bromine atom. Fluorine andchlorine are more preferred, particularly when the halogens aresubstituted on an alkyl (haloalkyl) or alkoxy group (e.g. CF₃ and CF₃O).It shall be understood that the respective denotation of Hal isindependently of one another in any radical of the invention.

In a preferred embodiment of the invention, the group Z in compounds offormula (I′) denotes H, F or OH.

In a most preferred embodiment of the invention, the group Z incompounds of formula (I′) denotes H.

R^(3′) denotes preferably H, methyl, ethyl, 2-hydroxyethyl or2-methoxyethyl.

Preferably, the group S(O)(NR^(3′)) is selected from

Preferably, the group N(SO)R^(3′) is selected from

A preferably denotes one of the following groups:

wherein R³, X, R′, R″ and R′″ have the meaning given above.

If A denotes

wherein R′″ and X have the meaning given above, it is preferably

If A denotes

wherein R′, R″ and X have the meaning given above, it is preferably

If A denotes

wherein R′, X and Y have the meaning given above, it is preferably

A is especially preferred one of the following groups:

The group Q preferably denotes H or one of the following groups:

wherein X, R′″, R³, T, Z⁵, Z⁶, R⁶ and R⁷ have the meaning given above.

R, R⁵, R⁶ and R⁷ are preferably independently H, CN, SO₂CH₃, SO₂CH₂CH₃,SO₂CH₂CH₂OH, SO₂CH₂CH₂OCH₃, S(O)(NR^(3′))CH₃, S(O)(NR^(3′))CH₂CH₃,S(O)(NR^(3′))CH₂CH₂OH, S(O)(NR^(3′))CH₂CH₂OCH₃, N(SO)R^(3′)CH₃,N(SO)R^(3′)CH₂CH₃, N(SO)R^(3′)CH₂CH₂OH, N(SO)R^(3′)CH₂CH₂OCH₃,

Hal, NR³R⁴, NO₂, phenyl, benzyl, CH₂-pyridyl, O-phenyl, O-pyridyl,O-pyrimidinyl, O-benzyl, 2-, 3- or 4-hydroxy or methoxyphenyl, alkyl,alkoxy (Oalkyl), hydroxyalkylen, alkoxyalkylen, COOH, COOalkyl,CONHalkyl, CONH₂, CON(CH₃)₂, NHCOalkyl, NHCOCH₃, NHCOphenyl,NHCOpyridyl, NHCH₂CH₃, NHCH₂CH₂CH₃, NHCOCH₂CH₂OH, CO—N-morpholinyl,CON(CH₃)CH₂CH₂N(CH₃)₂, CO-1-piperidinyl, CO-4-hydroxy-1-piperidinyl,CO-1-piperazinyl, CO-4-methyl-1-piperazinyl, CH₂—N-morpholinyl,CH₂N(H)COCH₃, CH₂N(CH₃)COCH₃, CH₂NH₂, NH₂, CH(OH)CH₃, CH(OR³)CH₃ or agroup selected from

wherein t+q is 2 or 3, preferably a group selected from

Preferably, one of the groups R′″, R″″, R⁵, R⁶ and R⁷ is a groupselected from:

Preferred are compounds of formula I, wherein only one of the groupsR′″, R″″, R⁵, R⁶ and R⁷ contains a group S(O)(NR^(3′)), N(SO)R^(3′),

More preferred are compounds of formula I, wherein one of the groups R⁵,R⁶ and R⁷ contains the group S(O)(NH), S(O)(NR^(3′)) or N(SO)R^(3″),

while the others of these groups denote H or methyl.

R⁸ is preferably a group selected from H, COalkyl or alkyl or hydroxylalkyl. More preferably, R⁸ is H, COmethyl or methyl, CON(SO)R^(3′)CH₃,CON(SO)R^(3′)CH₂CH₃, CON(SO)R^(3′)CH₂CH₂OH, CON(SO)R^(3′)CH₂CH₂OCH₃,S(O)(NH)CH₃, S(O)(NR^(3′))CH₃, S(O)(NR^(3′))CH₂CH₃,S(O)(NR^(3′))CH₂CH₂OH, S(O)(NR^(3′))CH₂CH₂OCH₃,

more preferably wherein R^(3′) is H or methyl.

X denotes preferably N or CH.

Y is preferably O or S.

R′, R″ denote each independently preferably H, methyl or ethyl. Morepreferred are compounds of formula I, wherein both R′, R″ aresimultaneously H or wherein one of the groups is H and the other groupis a straight chain or branched alkyl having 1 to 12 carbon atoms, morepreferably methyl or ethyl.

In preferred embodiments, R′″ denotes H, Hal or CN.

T is preferably N or CH, most preferably N.

Z¹ is preferably S or NH.

Z², Z³ preferably denote independently CH or N.

Z⁴ is preferably N or CH.

Z⁵ is preferably NR⁸, CHR⁵, S(O)(NR^(3′)), N(SO)R³, more preferably

Z⁶ is preferably CH₂, CO, SO₂ or

Z⁷ is preferably CH₂, S, O, NH. If Z⁷ is S, O, NR^(3′), t and q are each1 or one of t and q is 1 while the other denotes 2.

Most preferably, t and q simultaneously denote 1.

Compounds of formula I are further preferred,

-   -   wherein    -   A is preferably selected from one of the following groups:

-   -   and    -   the group Q is preferably selected from H or one of the        following groups:

-   -   wherein X, Y, R′, R″, R′″, R^(3′), R⁷ are as defined above,    -   and pharmaceutically usable derivatives, solvates, salts,        prodrugs, tautomers, enantiomers, racemates and stereoisomers        thereof, including mixtures thereof in all ratios and compounds        of formula I, wherein one or more H atoms may be replaced by D        (deuterium).

Throughout the specification and claims, the individual groups such asCOO, CONR³,

can be attached through any of the linking atoms to the rest of thecompound of formula I, i.e. a respective part of the compound of formulaI may be attached to the right or left or lower or upper side of theindividual group as presented in the specification.

Accordingly, the subject-matter of the invention relates to compounds offormula (I′) or (I) as medicament, in which at least one of theaforementioned radicals has any meaning, particularly realize anypreferred embodiment, as described above. Radicals, which are notexplicitly specified in the context of any embodiment of formula (I′) or(I), sub-formulae thereof or other radicals thereto, shall be construedto represent any respective denotations according to formula (I′) or (I)as disclosed hereunder for solving the problem of the invention. Thatmeans that the aforementioned radicals may adopt all designated meaningsas described in the present specification, irrespective of the contextto be found, including, but not limited to, any preferred embodiments.It shall be particularly understood that any embodiment of a certainradical can be combined with any embodiment of one or more otherradicals.

Particularly highly preferred embodiments are those compounds of formula(I′) or (I) listed in Table 1 and/or physiologically acceptable saltsthereof.

TABLE 1 Compounds of formulae (I′) or (I). OGA enzyme inhibition assay:OGA Optical Configuration IC50 No Structure rotation specification (M) 1

Racemic ++++ 2

[α]²⁴ _(D) = −11.00; c 0.10 (MeOH) First elution on Chiralcel OJ- H (250× 4.6)mm, 5 μm, 20 mM, 0.5% Isopropyl amine in IPA, Rt 2.97, Theenantiomeric purity is 99.1%. ++++ 3

Second elution on Chiralcel OJ-H (250 × 4.6)mm, 5 μm, 20 mM, 0.5%Isopropyl amine in IPA, Rt 3.43, The enantiomeric purity is 99.2%. + 4

Racemic ++++ 5

[α]²⁶ _(D) = −0.35; c 0.56 (MeOH) First elution on YMC Amylose-C (250 ×4.6)mm, 5 μm, 20 mM, 0.5% Isopropyl amine in methanol, Rt 4.56, Theenantiomeric purity is 100% ++++ 6

Second elution on YMC Amylose-C (250 × 4.6)mm, 5 μm, 20 mM, 0.5%Isopropyl amine in methanol, Rt 5.58, The enantiomeric purity is 98.1%.++ 7

Racemic ++++ 8

[α]²⁶ _(D) = −6.92; c 0.13 (MeOH) First elution on Lux A1 (250 × 4.6)mm,5 μm, 20 mM, 0.5% Isopropyl amine in methanol, Rt 2.96, The enantiomericpurity is 100% ++++ 9

Second elution on Lux A1 (250 × 4.6)mm, 5 μm, 20 mM, 0.5% Isopropylamine in methanol, Rt 4.09, The enantiomeric purity is 96.9%. +++ 10

Racemic +++ 11

Racemic ++++ 12

Racemic ++++ 13

Racemic ++ 14

Racemic ++++ 15

Racemic ++ 16

Racemic ++++ 17

Racemic ++ 18

Racemic ++++ 19

Racemic +++ 20

Racemic ++++ 21

[α]²⁶ _(D) = −3.77; c 0.52 (MeOH) First elution on Chiralcel OD- H (250× 4.6)mm, 5 μm, 20 mM, 0.5% isopropylamine in methanol, Rt 4.21 min, Theenantiomeric purity is 100.00%. ++++ 22

[α]²⁶ _(D) = 1.78; c 0.51 (MeOH) Second elution on Chiralcel OD-H (250 ×4.6)mm, 5 μm, 20 mM, 0.5% isopropylamine in methanol, Rt 4.58 min, Theenantiomeric purity is 97.33%. ++ 23

Racemic ++++ 24

Racemic ++++ 25

Racemic +++ 26

Racemic ++ 27

Second elution on Chiralcel OD-H (250 × 4.6)mm, 5 μm, 20 mM, 0.5%isopropylamine in methanol, Rt 4.07 min, The enantiomeric purity is99.59%. ++ 28

Racemic + 29

Racemic + 30

Racemic + 31

Racemic ++++ 32

Racemic + 33

Racemic ++++ 34

Racemic ++++ 35

36

37

Racemic ++++ 38

39

40

41

42

43

Racemic ++++ 44

45

46

47

48

49

50

51

Racemic ++++ 52

Racemic ++++ 53

54

55

56

57

58

59

60

Racemic ++++ 61

62

Racemic ++++ 63

64

65

66

67

68

69

70

71

72

73

74

75

76

77

78

79

80

81

82

83

84

85

86

87

88

89

90

91

92

Racemic ++++ 93

94

95

96

97

98

99

100

101

102

103

104

105

106

Racemic ++ 107

Racemic ++ 108

Racemic ++++ 109

Racemic ++++ 110

Racemic ++ 111

Racemic ++++ 112

Racemic ++ 113

First elution on YMC Amylose-SA (250 × 4.6)mm, 5 μm, 0.5% isopropylaminein methanol, Rt 4.79 min, Enantiomeric purity is 100.00%. ++++ 114

Second elution on YMC Amylose- SA (250 × 4.6)mm, 5 μm, 0.5%isopropylamine in methanol, Rt 5.60 min, Enantiomeric purity is 100.00%.++++ 115

Third elution on YMC Amylose- SA (250 × 4.6)mm, 5 μm, 0.5%isopropylamine in methanol, Rt 7.41 min, Enantiomeric purity is96.20%. + 116

Racemic +++ 117

Racemic ++++ 118

First elution on Chiralcel OD-H (250 × 4.6)mm, 5 um, 20 mM, 0.5%isopropylamine in isopropanol, Rt 4.09 min. Enantiomeric purity =99.13% + 119

Second elution on Chiralcel OD-H (250 × 4.6)mm, 5 um, 20 mM, 0.5%isopropylamine in isopropanol, Rt 4.64 min. Enantiomeric purity = 97.12%++++ 120

Racemic ++++ 121

Racemic ++ 122

Racemic + 123

124

125

126

127

128

129

130

131

132

133

Activity range of the compounds of Formula (I′) or (I) is the following:

+ 1 to 10 μM

++ 0.2 to 1 μM

+++ 0.2 to 0.05 μM

++++ below 0.05 μM

Further preferred compounds of the invention are the following:

Structure

Preferred compounds of the present invention demonstrate adequateproperties for use as a drug. In particular, such preferred compoundsshow a high solid state stability, high stability in the presence ofliver microsome, high oxidation stability and suitable permeability.Further preferred compounds of the present invention demonstrate theirsuitability as drugs by potent biological activity, such as the level ofO-GlcNAcylation of total proteins measured in brain extracts. Relevanttests for determining such parameters are known by the person skilled inthe art, e.g. solid state stability (Waterman K. C. (2007) Pharm Res24(4); 780-790), stability in the presence of liver microsome (Obach R.S. (1999) Drug Metab Dispos 27(11); 1350-135) and the permeability (e.g.Caco-2 permeability assay, Calcagno A. M. (2006) Mol Pharm 3(1); 87-93);alternatively, they are described in Examples below, such as Example B02describing the determination of O-GlcNAcylation level of total proteinsmeasured in brain extracts. Compounds of the present invention that showa high potency in OGA inhibition assays and one or more of the aboveproperties are especially suitable as a drug for the indicationsmentioned in the present specification.

The compounds according to formula (I′) or (I) and the startingmaterials for its preparation, respectively, are produced by methodsknown per se, as described in the literature, i.e. under reactionconditions that are known and suitable for said reactions.

Use can also be made of variants that are known per se, but are notmentioned in greater detail herein. If desired, the starting materialscan also be formed in-situ by leaving them in the un-isolated status inthe crude reaction mixture, but immediately converting them further intothe compound according to the invention. On the other hand, it ispossible to carry out the reaction Step wise.

The following abbreviations refer respectively to the definitions below:Ac (acetyl), aq (aqueous), h (hour), g (gram), L (liter), mg(milligram), MHz (Megahertz), μM (micromolar), min (minute), mm(millimeter), mmol (millimole), mM (millimolar), m.p. (melting point),equiv (equivalent), mL (milliliter), μL (microliter), ACN(acetonitrile), AcOH (acetic acid), BINAP(2,2′-bis(disphenylphosphino)-1,1′-binaphthalene, BOC(tert-butoxy-carbonyl), CBZ (carbobenzoxy), CDCl₃ (deuteratedchloroform), CD₃OD (deuterated methanol), CH₃CN (acetonitrile), c-hex(cyclohexane), DCC (dicyclohexyl carbodiimide), DCM (dichloromethane),DHP (O-(2,4-dinitrophenyl)-hydroxylamine), dppf(1,1′-bis(diphenylphosphino)ferrocene), DIC (diisopropyl carbodiimide),DIEA (diisopropylethyl-amine), DMF (dimethylformamide), DMSO(dimethylsulfoxide), DMSO-d₆ (deuterated dimethylsulfoxide), EDC(1-(3-dimethyl-amino-propyl)-3-ethylcarbodiimide), ESI (Electro-sprayionization), EtOAc (Ethyl acetate), Et₂O (diethyl ether), EtOH(ethanol), FMOC (fluorenylmethyloxycarbonyl), HATU(dimethylamino-([1,2,3]triazolo[4,5-b]pyridin-3-yloxy)-methylene]-dimethyl-ammoniumhexafluorophosphate), HPLC (High Performance Liquid Chromatography),i-PrOH (2-propanol), K₂CO₃ (potassium carbonate), LC (LiquidChromatography), m-CPBA (3-chloroperbenzoic acid), MD Autoprep (Massdirected Autoprep), MeOH (methanol), MgSO₄ (magnesium sulfate), MS (massspectrometry), MSH (O-mesitylenesulfonylhydroxylamine), MTBE (Methyltert-butyl ether), Mtr. (4-Methoxy-2, 3, 6-trimethylbenzensulfonyl), MW(microwave), NBS (N-bromo succinimide), NaHCO₃ (sodium bicarbonate),NaBH₄ (sodium borohydride), NMM (N-methyl morpholine), NMR (NuclearMagnetic Resonance), POA (phenoxyacetate), Py (pyridine), PyBOP®(benzotriazole-1-yl-oxy-tris-pyrrolidino-phosphoniumhexafluorophosphate), RT (room temperature), Rt (retention time), SFC(supercritical fluid chromatography), SPE (solid phase extraction), T3P(propylphosphonic anhydride), TBAF (tetra-n-butylammonium fluoride),TBTU (2-(1-H-benzotriazole-1-yl)-1,1,3,3-tetramethyluromium tetrafluoroborate), TEA (triethylamine), TFA (trifluoroacetic acid), THE(tetrahydrofurane), TLC (Thin Layer Chromatography), UV (Ultraviolet).

In general, the compounds according to Formula (I′) or (I) and relatedformulae of this invention may be prepared from readily availablestarting materials. If such starting materials are not commerciallyavailable, they may be prepared by standard synthetic techniques. Ingeneral, the synthesis pathways for any individual compound of Formula(I′) or (I) and related formulae will depend on the specificsubstituents of each molecule, such factors being appreciated by thosehaving ordinary skill in the art. The following general methods andprocedures described hereinafter in the examples may be employed toprepare compounds of Formula (I′) or (I) and related formulae. Reactionconditions depicted in the following schemes, such as temperatures,solvents, or co-reagents, are given as examples only and are notrestrictive. It will be appreciated that where typical or preferredexperimental conditions (i.e. reaction temperatures, time, moles ofreagents, solvents etc.) are given, other experimental conditions canalso be used unless otherwise stated. Optimum reaction conditions mayvary with the particular reactants or solvents used, but such conditionscan be determined by a person skilled in the art, using routineoptimisation procedures. For all the protection and deprotectionmethods, see Philip J. Kocienski, in “Protecting Groups”, Georg ThiemeVerlag Stuttgart, N.Y., 1994 and, Theodora W. Greene and Peter G. M.Wuts in “Protective Groups in Organic Synthesis”, Wiley Interscience,3^(rd) Edition 1999.

A “leaving group” LG denotes a chemical moiety which can be removed orreplaced by another chemical group. Throughout the specification, theterm leaving group preferably denotes Cl, Br, I or a reactively modifiedOH group, such as, for example, an activated ester, an imidazolide oralkylsulfonyloxy having 1 to 6 carbon atoms (preferablymethylsulfonyloxy or trifluoromethylsulfonyloxy) or arylsulfonyloxyhaving 6 to 10 carbon atoms (preferably phenyl- or p-tolylsulfonyloxy).When a leaving group LG is attached to an aromatic or heteroaromaticring, LG can denote in addition SO₂-alkyl or F. Radicals of this typefor activation of the carboxyl group in typical acylation reactions aredescribed in the literature (for example in the standard works, such asHouben-Weyl, Methoden der organischen Chemie [Methods of OrganicChemistry], Georg-Thieme-Verlag, Stuttgart). Activated esters areadvantageously formed in situ, for example through addition of HOBt,N-hydroxysuccinimide or HATU.

Depending on the nature of A, R¹, R², T¹, T², T³, T⁴, L, W, Z, R′″, mand n different synthetic strategies may be selected for the synthesisof compounds of Formula (I′) or (I). In the process illustrated in thefollowing schemes, A, R¹, R², T¹, T², T³, T⁴, L, W, Z, R′″, m and n areas above-defined in the description unless otherwise mentioned.

Compounds of Formula (I′) or (I), wherein A, R¹, R², T¹, T², T³, T⁴, L,W, Z, R′″, m and n are defined as above, can be prepared fromalternative compounds of Formula (I′) or (I), using suitableinterconversion procedures such as those described hereinafter in theexamples, or conventional interconversion procedures well known by oneskilled in the art.

Compound of formula (I′) or (I), isolated as a mixture of compounds offormula (Ia′), (Ib′), (Ic′) and (Id′) or (Ia), (Ib), (Ic) and (Id) insame or different ratio, can be separated into compounds of formula(Ia′), (Ib′), (Ic′) and (Id′) or (Ia), (Ib), (Ic) and (Id) by chiralchromatography or by chiral resolution, re-crystallization with use ofan optically active acid, using methods known by one skilled in the artand as described below in the examples (Scheme 1′ and Scheme 1).

Compounds of formula (I′) or (I), wherein A, R¹, R², T¹, T², T³, T⁴, L,W, Z, R′″, m and n are defined as above, can be prepared fromalternative compounds of formula (I′) or (I), depending on the nature ofL, Z and W, using methods and reactions known by a person skilled in theart. Such reactions can be but are not limited to aromatic substitution,alkylation, metal catalyzed cross-coupling reaction.

Compounds of formula (I′) or (I), wherein A, R¹, R², T¹, T², T³, T⁴, L,W, Z, R′″, m and n are defined as above, can be prepared from thecorresponding amine (V′) or (V) by reductive amination with ketone (II),using conditions known to the one skilled in the art, such as but notlimited to the use of NaBH(OAc)₃ as reducing agent, in the presence ofone equivalent of AcOH in DCE (Scheme 2). Alternatively, reductiveamination can be performed in two steps, with first imine formation,that can be catalysed by Ti(OiPr)₄, followed by reduction with suitablereducing agent, such as but not limited to NaBH₄ in MeOH (Abdel-Magid,A. F. at al. J. Org. Chem. 1996, 61, 3849-3862). Alternatively, ketone(II) can be reduced into the corresponding alcohol (Ill) using usualreductive agents such as NaBH₄ in an alcoholic solvent, such as MeOH.Alcohol functionality can be then transformed into a suitable leavinggroup, such as but not limited to Cl or OMs, using conditions known by aperson skilled in the art. Addition of amines (V′) or (V) tointermediates (IV) yields the formation of compounds (I′) or (I) (Scheme2′ and Scheme 2).

Compounds of formula (V′) or (V) can be separated into compounds offormula (Va′) and (Vb′) or (Va) and (Vb) by chiral chromatography orchiral resolution by re-crystallization with an optically active acid,using methods known by one skilled in the art and as described below inthe examples (Scheme 3′ and Scheme 3).

Amines of formula (V) can be synthesized from different precursors,depending on the nature of wherein R², T¹, T², T³, T⁴, L, W, R′″, m andn, using methods known by a person skilled in the art. Amines of formula(Vc) and (Vd) can be obtained from ketone of formula (VIII), wherein T¹,T², T³, T⁴, L, W and R′″ are defined as above. Intramolecular Schmidtreaction of ketone of formula (VIII), using conditions known by a personskilled in the art, yields lactams of formula (IXc) and (IXd) (Aube, J.et al. J. Am. Chem. Soc. 1991, 113, 8965-8966; J. Am. Chem. Soc. 2000,122, 7226-7232). Their reduction, with but not limited to BH₃, allowsthe isolation of amine of formula (Vc) and (Vd) (Scheme 4).

Alternatively, amine of formula (Ve) can be obtained through amulti-Step synthesis, as depicted on Scheme 6. Coupling of acid (X) withamino ester (XI), wherein R¹, T¹, T², T³, T⁴, L, W and R′″ are definedas above, gives compound of formula (XII). Reduction of compound offormula (XII) into the corresponding aldehyde (XIII), followed by acetal(XIV) formation and cyclization, yield compound of formula (XV). Amineof formula (Ve) can be finally obtained after double bond and lactamereduction (Scheme 5).

Amine of formula (Ve) can be obtained through an alternative multi-stepsynthesis, as depicted on Scheme 6. Metal catalysed coupling of (XVII)with (XVI) (when R²═H, see Molander, G. A. et al J. Org. Chem. 2012, 77,10399-10408), followed by cyclization with protected ammonia H₂NPGyields amine of formula (XIX). Amine of formula (Ve) can be obtainedafter cleavage of the protecting group PG.

Alternatively, amines of formula (Vf′) and (Vg′), wherein Z is OH or Halrespectively, can be obtained through a multi-Step synthesis, asdepicted on Scheme 7. Reduction of acid (X) would yield alcohol (XX)that can react with protected amine (XXI), where PG is a protectinggroup selected from but not limited to Boc or tosyl, under Mistunobuconditions. After ester (XXII) hydrolysis under basic conditions, theresulting acid (XXIII) is cyclized in the presence of a Lewis acid, suchas but not limited to SnCl₄ and trifluoroacetic anhydride. Aftercyclization, amine (XXIV) can be reduced into alcohol (XXV) that can befurther transformed into halogenated analogues (XXVI), such asfluorinated analogues (XXVIa) if DAST is used as reagent. Deprotectionof compound (XXV) or (XXVI) is yielding amines of formula (Vf′) and(Vg′) wherein Z is OH or Hal respectively.

Compounds of formula (V′), (V) or (XIX), wherein R², T¹, T², T³, T⁴, L,W, Z, R′″, m and n are defined as above, can be prepared fromalternative compounds of formula (V′), (V) or (XIX), depending on thenature of L, Z and W, using methods and reactions known by a personskilled in the art. Such reactions can be, but are not limited to,aromatic substitution, alkylation, metal catalyzed cross-couplingreaction.

Alternatively aldehyde of formula (XXVII) can be transformed intoalcohol of formula (VI) with addition of a suitable nucleophile, such asbut not limited to a Grignard reagent (Scheme 8).

In another process, ketone of formula (IVa) can be obtained by Stillecross coupling reaction between aryl halide (XXVIII) andtributyl(1-ethoxyvinyl)tin in the presence of a catalyst, such as butnot limited to Pd(PPh₃)₂Cl₂ in toluene at temperatures ranging from RTto 110° C. (Scheme 9).

The sulfoximine group and related functionalities as indicated in thedefinitions can be introduced or generated at any stage of the synthesisof compounds of formula (I′) or (I), as described below in the examplesusing methods known by one skilled in the art (Frings, M. et al. Eur. J.Med. Chem. 2017, 126, 225-245 and cited references).

When a reaction is preferably performed under basic conditions, asuitable base might be selected from metal oxides, e.g. aluminum oxide,alkaline metal hydroxide (potassium hydroxide, sodium hydroxide andlithium hydroxide, inter alia), alkaline earth metal hydroxide (bariumhydroxide and calcium hydroxide, inter alia), alkaline metal alcoholates(potassium ethanolate and sodium propanolate, inter alia), alkalinemetal carbonates (e.g., sodium bicarbonate) and several organic bases(e.g., N,N-diisopropylethylamine, piperidine or diethanolamine, interalia).

The reaction is generally carried out in an inert solvent. Suitableinert solvents are, for example, hydrocarbons, such as hexane, petroleumether, benzene, toluene or xylene; chlorinated hydrocarbons, such astrichloroethylene, 1,2-dichloroethane, carbon tetrachloride, chloroformor dichloromethane; alcohols, such as methanol, ethanol, isopropanol,n-propanol, n-butanol or tert-butanol; ethers, such as diethyl ether,diisopropyl ether, tetrahydrofuran (THF) or dioxane; glycol ethers, suchas ethylene glycol monomethyl or monoethyl ether, ethylene glycoldimethyl ether (diglyme); ketones, such as acetone or butanone; amides,such as acetamide, dimethylacetamide or dimethylformamide (DMF);nitriles, such as acetonitrile; sulfoxides, such as dimethyl sulfoxide(DMSO); carbon disulfide; carboxylic acids, such as formic acid, aceticacid or trifluoroacetic acid (TFA); nitro compounds, such asnitromethane or nitrobenzene; esters, such as ethyl acetate, or mixturesof the said solvents. Particular preference is given to TFA, DMF,dichloromethane, THF, H₂O, methanol, tert. butanol, tert. amylalcohol,triethylamine or dioxane.

Depending on the conditions used, the reaction time is between a fewminutes and 14 days, the reaction temperature is between about −80° C.and 140° C., normally between −50° C. and 120° C., preferably between−20° C. and 100° C.

The compounds of formula (I′) or (I) and sub-formulae thereof areaccessible via the routes above. The starting materials, are usuallyknown to the skilled artisan, or they can be easily prepared by knownmethods.

The compounds of formula (I′) or (I) can be modified, like hydrogenatedor metal-reduced, to remove the chlorine, or put into a substitutionreaction, and/or to be transformed with an acid or base into a salt,preferably with a strong acid. Numerous papers and methods are availableand useful for the one skilled in the art in respect for organicchemistry, chemical strategies and tactics, synthetic routes, protectionof intermediates, cleavage and purification procedure, isolation andcharacterization. General chemical modifications are known to the oneskilled in the art. Halogenation of aryls or hydroxy substitution byhalogens of acids, alcohols, phenols, and their tautomeric structurescan be preferably carried out by use of POCl₃, or SOCl₂, PCI₅, SO₂Cl₂.In some instances oxalyl chloride is also useful. Temperatures can varyfrom 0° C. to reflux depending on the task to halogenate a pyridonestructure or a carboxylic acid or a sulfonic acid. Time will also beadjusted from minutes to several hours or even over night. Similarly,alkylation, ether formation, ester formation, amide formation are knownto the one skilled in the art. Arylation with aryl boronic acids can beperformed in presence of a Pd catalyst, appropriate ligand and base,preferably a carbonate, phosphate, borate salt of sodium, potassium orcesium. Organic bases, like Et₃N, DIPEA or the more basic DBU can alsobe used. Solvents can vary too, from toluene, dioxane, THF, diglyme,monoglyme, alcohols, DMF, DMA, NMP, acetonitrile, in some cases evenwater, and others. Commonly used catalysts like Pd (PPh₃)₄, or Pd(OAc)₂,PdCl₂ type precursors of PdO catalysts have advanced to more complexones with more efficient ligands. In C—C arylations, instead of boronicacids and esters, aryl-trifluoroborate potassium salts (Suzuki-Miyauracoupling), organo silanes (Hiyama coupling), Grignard reagents (Kumada),organozinc compounds (Negishi coupling) and stannanes (Stille coupling)may be useful. This experience can be transferred to N- andO-arylations. Numerous papers and methods are available and useful forthe one skilled in the art in respect of N-arylation and even ofelectron deficient anilines, and with aryl chlorides and anilines aswell as for O-arylation by using Cu catalysis and Pd catalysis.

In the final Step of the processes above, a salt of the compounds,preferably those of formula (I′) or (I), is optionally provided. Thesaid compounds according to the invention can be used in their finalnon-salt form. On the other hand, the present invention also encompassesthe use of these compounds in the form of their pharmaceuticallyacceptable salts, which can be derived from various organic andinorganic acids and bases by procedures known in the art.Pharmaceutically acceptable salt forms of the compounds according to theinvention are for the most part prepared by conventional methods. If thecompound according to the invention contains a carboxyl group, one ofits suitable salts can be formed by the reaction of the compound with asuitable base to give the corresponding base-addition salt. Such basesare, for example, alkali metal hydroxides, including potassiumhydroxide, sodium hydroxide and lithium hydroxide; alkaline earth metalhydroxides, such as magnesium hydroxide, calcium hydroxide and bariumhydroxide; alkali metal alkoxides, for example potassium ethoxide andsodium propoxide; and various organic bases, such as piperidine,diethanolamine and N-methyl-glucamine (meglumine), benzathine, choline,diethanolamine, ethylenediamine, benethamine, diethylamine, piperazine,lysine, L-arginine, ammonia, triethanolamine, betaine, ethanolamine,morpholine and tromethamine. The aluminum salts of the compoundsaccording to the invention are likewise included. In the case of certaincompounds of the formula I, which contain a basic center, acid-additionsalts can be formed by treating these compounds with pharmaceuticallyacceptable organic and inorganic acids, for example hydrogen halides,such as hydrogen chloride, hydrogen bromide or hydrogen iodide, othermineral acids and corresponding salts thereof, such as sulfate, nitrateor phosphate and the like, and alkyl- and monoarylsulfonates, such asmethanesulfonate, ethanesulfonate, toluenesulfonate andbenzenesulfonate, and other organic acids and corresponding saltsthereof, such as carbonate, acetate, trifluoroacetate, tartrate,maleate, succinate, citrate, benzoate, salicylate, ascorbate and thelike. Accordingly, pharmaceutically acceptable acid-addition salts ofthe compounds according to the invention include the following: acetate,adipate, alginate, arginate, aspartate, benzoate, benzenesulfonate(besylate), bisulfate, bisulfite, bromide, butyrate, camphorate,camphorsulfonate, caprate, caprylate, chloride, chlorobenzoate, citrate,cyclamate, cinnamate, cyclopentanepropionate, digluconate,dihydrogenphosphate, dinitrobenzoate, dodecylsulfate, ethanesulfonate,formate, glycolate, fumarate, galacterate (from mucic acid),galacturonate, glucoheptanoate, gluconate, glutamate, glycerophosphate,hemisuccinate, hemisulfate, heptanoate, hexanoate, hippurate,hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate,iodide, isethionate, isobutyrate, lactate, lactobionate, malate,maleate, malonate, mandelate, metaphosphate, methanesulfonate,methylbenzoate, monohydrogenphosphate, 2-naphthalenesulfonate,nicotinate, nitrate, oxalate, oleate, palmoate, pectinate, persulfate,phenylacetate, 3-phenylpropionate, phosphate, phosphonate, phthalate,but this does not represent a restriction.

Both types of salts may be formed or interconverted preferably usingion-exchange resin techniques.

With regard to that stated above, it can be seen that the expressions“pharmaceutically acceptable salt” and “physiologically acceptablesalt”, which are used interchangeable herein, in the present connectionare taken to mean an active ingredient which comprises a compoundaccording to the invention in the form of one of its salts, inparticular if this salt form imparts improved pharmacokinetic propertieson the active ingredient compared with the free form of the activeingredient or any other salt form of the active ingredient used earlier.The pharmaceutically acceptable salt form of the active ingredient canalso provide this active ingredient for the first time with a desiredpharmacokinetic property which it did not have earlier and can even havea positive influence on the pharmacodynamics of this active ingredientwith respect to its therapeutic efficacy in the body.

The above-mentioned pharmaceutical salts which are preferred includeacetate, trifluoroacetate, besylate, citrate, fumarate, gluconate,hemisuccinate, hippurate, hydrochloride, hydrobromide, isethionate,mandelate, me-glumine, nitrate, oleate, phosphonate, pivalate, sodiumphosphate, stearate, sulfate, sulfosalicylate, tartrate, thiomalate,tosylate and tro-meth-amine, but this is not intended to represent arestriction.

The acid-addition salts of basic compounds of the formula (I′) or (I)are prepared by bringing the free base form into contact with asufficient amount of the desired acid, causing the formation of the saltin a conventional manner. The free base can be regenerated by bringingthe salt form into contact with a base and isolating the free base in aconventional manner. The free base forms differ in a certain respectfrom the corresponding salt forms thereof with respect to certainphysical properties, such as solubility in polar solvents; for thepurposes of the invention, however, the salts other-wise correspond tothe respective free base forms thereof.

As mentioned, the pharmaceutically acceptable base-addition salts of thecompounds of the formula I are formed with metals or amines, such asalkali metals and alkaline earth metals or organic amines. Preferredmetals are sodium, potassium, magnesium and calcium. Preferred organicamines are N,N′-dibenzylethylenediamine, chloroprocaine, choline,diethanol-amine, ethylenediamine, N-methyl-D-glucamine and procaine.This is not intended to represent a restriction.

The base-addition salts of acidic compounds of the formula I areprepared by bringing the free acid form into contact with a sufficientamount of the desired base, causing the formation of the salt in aconventional manner. The free acid can be regenerated by bringing thesalt form into contact with an acid and isolating the free acid in aconventional manner. The free acid forms differ in a certain respectfrom the corresponding salt forms thereof with respect to certainphysical properties, such as solubility in polar solvents; for thepurposes of the invention, however, the salts other-wise correspond tothe respective free acid forms thereof.

If a compound of the formula (I′) or (I) contains more than one groupwhich is capable of forming pharmaceutically acceptable salts of thistype, the formula I also encompasses multiple salts. Typical multiplesalt forms include, for example, bitartrate, diacetate, difumarate,dimeglumine, di-phosphate, disodium and trihydrochloride, but this isnot intended to represent a restriction.

With regard to that stated above, it can be seen that the expressions“pharmaceutically acceptable salt” and “physiologically acceptablesalt”, which are used interchangeable herein, in the present connectionare taken to mean an active ingredient which comprises a compoundaccording to the invention in the form of one of its salts, inparticular if this salt form imparts improved pharmacokinetic propertieson the active ingredient compared with the free form of the activeingredient or any other salt form of the active ingredient used earlier.The pharmaceutically acceptable salt form of the active ingredient canalso provide this active ingredient for the first time with a desiredpharmacokinetic property which it did not have earlier and can even havea positive influence on the pharmacodynamics of this active ingredientwith respect to its therapeutic efficacy in the body.

Owing to their molecular structure, the compounds of the formula (I′) or(I) can be chiral and can accordingly occur in various enantiomericforms. They can therefore exist in racemic or in optically active form.

Since the pharmaceutical activity of the racemates or stereoisomers ofthe compounds according to the invention may differ, it may be desirableto use the enantiomers. In these cases, the end product or even theIntermediates can be separated into enantiomeric compounds by chemicalor physical measures known to the person skilled in the art or evenemployed as such in the synthesis.

In the case of racemic amines, diastereomers are formed from the mixtureby reaction with an optically active resolving agent. Examples ofsuitable resolving agents are optically active acids, such as the (R)and (S) forms of tartaric acid, diacetyltartaric acid, dibenzoyltartaricacid, di-O-β-toluoyl-tartaric acid, mandelic acid, malic acid, lacticacid, suitable N-protected amino acids (for example N-benzoylproline orN-benzenesulfonylproline), or the various optically activecamphorsulfonic acids. The suitably formed salt with optically activeacid is crystallized using various combinations of solvents, such as butnot limited to methanol, ethanol, isopropanol, THF, water, diethylether, acetone, methyl tert-butyl ethers and other solvents known to theperson skilled in the art. Also advantageous is chromatographicenantiomer resolution with the aid of an optically active resolvingagent (for example dinitrobenzoylphenylglycine, cellulose triacetate orother derivatives of carbohydrates or chirally derivatised methacrylatepolymers immobilised on silica gel). Suitable eluents for this purposeare aqueous or alcoholic solvent mixtures, such as, for example,hexane/isopropanol/acetonitrile, for example in the ratio 82:15:3.

When discovering and developing therapeutic agents, the person skilledin the art attempts to optimize pharmacokinetic parameters whileretaining desirable in-vitro properties. It is reasonable to assume thatmany compounds with poor pharmacokinetic profiles are susceptible tooxidative metabolism. In-vitro liver microsomal assays currentlyavailable provide valuable information on the course of oxidativemetabolism of this type, which in turn permits the rational design ofdeuterated compounds of the formula (I′) or (I) with improved stabilitythrough resistance to such oxidative metabolism. Significantimprovements in the pharmacokinetic profiles of compounds of the formula(I′) or (I) are thereby obtained, and can be expressed quantitatively interms of increases in the in vivo half-life (t/2), concentration atmaximum therapeutic effect (C_(max)), area under the dose response curve(AUC), and F; and in terms of reduced clearance, dose and materialscosts.

A further aspect of the invention relates to the use of compoundsaccording to formula (I′) or (I) and/or physiologically acceptable saltsthereof for inhibiting a glycosidase. Such use may be therapeutic ornon-therapeuic in character. The term “inhibition” denotes any reductionin glycosidase activity, which is based on the action of the specificinventive compounds capable to interact with the target glycosidase insuch a manner that makes recognition, binding and blocking possible. Itshall be understood that the compounds of the invention finally interactwith the target to unfold the effect. The compounds are characterized bysuch an appreciable affinity to at least one glycoside hydrolase whichensures a reliable binding and preferably a complete blocking ofglycosidase activity. More preferably, the substances are mono-specificin order to guarantee an exclusive and directed recognition with thechosen single glycosidase target. In the context of the presentinvention, the term “recognition”—without being limited thereto—relatesto any type of interaction between the specific compounds and thetarget, particularly covalent or non-covalent binding or association,such as a covalent bond, hydrophobic/hydrophilic interactions, van derWaals forces, ion pairs, hydrogen bonds, ligand-receptor interactions,and the like. Such association may also encompass the presence of othermolecules such as peptides, proteins or nucleotide sequences. Thepresent receptor/ligand-interaction is preferably characterized by highaffinity, high selectivity and minimal or even lacking cross-reactivityto other target molecules to exclude unhealthy and harmful impacts tothe treated subject.

In a preferred embodiment of the present invention, the glycosidasecomprises glycoside hydrolases, more preferably family 84 glycosidehydrolases, most preferablyO-glycoprotein-2-acetamido-2deoxy-β-D-glucopyranosidase (OGA), highlypreferably a mammalian O-GlcNAcase. It is particularly preferred thatthe compounds of formula (I′) or (I) according to the inventionselectively bind an O-GlcNAcase, e.g. thereby selectively inhibiting thecleavage of 2-acetamido-2-deoxy-β-D-glucopyranoside (O-GlcNAc) whilethey do not substantially inhibit a lysosomal β-hexosaminidase.

The compounds according to the invention preferably exhibit anadvantageous biological activity, which is easily demonstrated in enzymeactivity assays as described herein or known from prior art. In suchin-vitro assays, the compounds preferably exhibit and cause aninhibitory effect. IC₅₀ is the concentration of a compound that produces50% of the maximal inhibition for that compound. The glycosidase targetis especially half inhibited by the compounds described herein if theconcentration of the compounds amounts to less than 100 μM, preferablyless than 10 μM, more preferably less than 1 μM, most preferably lessthan 0.2 μM. Most preferably, compounds of Formula (I′) or (I) exhibitan IC₅₀ less than 0.02 μM.

A further aspect of the present invention relates to a method forinhibiting a glycosidase, wherein a system capable of expressing theglycosidase, particularly expressing said glycosidase, is contacted withat least one compound of formula (I′) or (I) according to the inventionand/or physiologically acceptable salts thereof, under conditions suchthat said glycosidase is inhibited. In a preferred embodiment of themethod, the glycosidase is contacted with a compound selectivelyinhibiting O-GlcNAcase and more preferably having an IC₅₀ of less than0.2 μM. It is also preferred that the method is performed in-vitroand/or that the method is not practiced on the human body. A cellularsystem is preferred in the scope of the method. The cellular system isdefined to be any subject provided that the subject comprises cells. Thecell refers to any type of primary cells or genetically engineeredcells, whether in the isolated status, in culture, as cell line,assembled in tissue, organs or intact laboratory mammals, provided thatthey are capable of expressing the glycosidase. It shall also beunderstood that the cell expresses the glycosidase as inherentpre-condition to put the methods of inhibition into practice. Althoughit is particularly preferred that the cells are capable of expressing ordo express the glycosidase, it shall not be excluded thatglycosidase-deficient cells can be used and the glycosidase isartificially added to the cellular system. The assay of the inventioncan be even completely performed in-vitro such that the cell is waivedbut a glycosidase is contacted with at least one compound of formula(I′) or (I) according to the invention and/or physiologically acceptablesalts thereof. Hence, an amount of isolated glycosidase is provided incrude or purified form for this purpose.

As discussed herein, the glycosidase-signaling pathways are relevant forvarious diseases, preferably neurodegenerative diseases, diabetes,cancer, cardiovascular diseases and stroke. Accordingly, the compoundsaccording to the invention are useful in the prophylaxis and/ortreatment of diseases that are dependent on the said signaling pathwaysby interaction with one or more of them. The present invention thereforerelates to the therapeutic and non-therapeutic use of compoundsaccording to the invention as inhibitors of the signaling pathwaysdescribed herein, preferably of the OGA-mediated signaling.

The method of the invention can be performed either in-vitro or in-vivo.The susceptibility of a particular cell to treatment with the compoundsaccording to the invention can be particularly determined by in-vitrotests, whether in the course of research or clinical application.Typically, a culture of the cell is combined with a compound accordingto the invention at various concentrations for a period of time which issufficient to allow the active agents to modulate glycosidase activity,usually between about one hour and one week. In-vitro treatment can becarried out using cultivated cells from any sample or cell line.

The host or patient can belong to any mammalian species, for example aprimate species, particularly humans; rodents, including mice, rats andhamsters; rabbits; horses, cows, dogs, cats, etc. Animal models are ofinterest for experimental investigations, providing a model fortreatment of human disease.

For identification of a signal transduction pathway and for detection ofinteractions between various signal transduction pathways, variousscientists have developed suitable models or model systems, for examplecell culture models and models of transgenic animals. For thedetermination of certain stages in the signal transduction cascade,interacting compounds can be utilized in order to modulate the signal.The compounds according to the invention can also be used as reagentsfor testing OGA-dependent signal transduction pathways in animals and/orcell culture models or in the clinical diseases mentioned in thisapplication.

The use according to the previous paragraphs of the specification may beeither performed in-vitro or in-vivo models. The inhibition can bemonitored by the techniques described in the course of the presentspecification. The in-vitro use is preferably applied to samples ofhumans suffering from neurodegenerative diseases, diabetes, cancer,cardiovascular diseases and stroke. Testing of several specificcompounds and/or derivatives thereof makes the selection of that activeingredient possible that is best suited for the treatment of the humansubject. The in-vivo dose rate of the chosen derivative isadvantageously pre-adjusted to the glycosidase susceptibility and/orseverity of disease of the respective subject with regard to thein-vitro data. Therefore, the therapeutic efficacy is remarkablyenhanced. Moreover, the subsequent teaching of the present specificationconcerning the use of the compounds according to formula (I′) or (I) andits derivatives for the production of a medicament for the prophylacticor therapeutic treatment and/or monitoring is considered as valid andapplicable without restrictions to the use of the compound for theinhibition of glycosidase activity, preferably OGA activity, ifexpedient.

A further aspect of the invention relates to a medicament comprising atleast one compound according to the invention and/or pharmaceuticallyusable derivatives, salts, solvates and stereoisomers thereof, includingmixtures thereof in all ratios. A “medicament” in the meaning of theinvention is any agent in the field of medicine, which comprises one ormore compounds of formula (I′) or (I) or preparations thereof (e.g. apharmaceutical composition or pharmaceutical formulation) and can beused in prophylaxis, therapy, follow-up or aftercare of patients whosuffer from diseases, which are associated with OGA activity, in such away that a pathogenic modification of their overall condition or of thecondition of particular regions of the organism could establish at leasttemporarily.

Consequently, the invention also relates to a pharmaceutical compositioncomprising as active ingredient an effective amount of at least onecompound of formula (I′) or (I) according to the invention and/orphysiologically acceptable salts thereof together with pharmaceuticallytolerable adjuvants and/or excipients.

In the meaning of the invention, an “adjuvant” denotes every substancethat enables, intensifies or modifies a specific response against theactive ingredient of the invention if administered simultaneously,contemporarily or sequentially. Known adjuvants for injection solutionsare, for example, aluminum compositions, such as aluminum hydroxide oraluminum phosphate, saponins, such as QS21, muramyldipeptide ormuramyltripeptide, proteins, such as gamma-interferon or TNF, M59,squalen or polyols.

Furthermore, the active ingredient may be administered alone or incombination with other treatments. A synergistic effect may be achievedby using more than one compound in the pharmaceutical composition, i.e.the compound of formula (I′) or (I) is combined with at least anotheragent as active ingredient, which is either another compound of formula(I′) or (I) or a compound of different structural scaffold. The activeingredients can be used either simultaneously or sequentially. Thepresent compounds are suitable for combination with agents known tothose of skill in the art (e.g., WO 2008/025170) and are useful with thecompounds of the invention.

In some embodiments, a compound according to the invention, or for useaccording to the invention, may be provided in combination with anyother active agents or pharmaceutical compositions where such combinedtherapy may be useful to modulate O-GlcNAcase activity, for example totreat neurodegenerative, inflammatory, cardiovascular, orimmunoregulatory diseases or any condition described herein. In someembodiments, a compound according to the invention, or for use accordingto the invention, may be provided in combination with one or more agentsuseful in the prevention or treatment of tauopathies and Alzheimer'sdisease. Examples of such agents may include, without limitation,

-   -   Acetylcholine esterase inhibitors (AChEIs) such as Aricept®        (Donepezil), Exelon® (Rivastigmine), Razadyne® (Razadyne ER®,        Reminyl®, Nivalin®, Galantamine), Cognex® (Tacrine), NMDA        antagonists such as memantine (Axura®, Ebixa®), Huperzine A,        Phenserine, Debio-9902 SR (ZT-1 SR), Zanapezil (TAK0147),        ganstigmine, NP7557, α7 nicotinic acetylcholine receptor        agonists, 5-HT6 receptor antagonists, M1 muscarinic        acetylcholine receptor agonists and positive allosteric        modulators, etc    -   Tau aggregation inhibitors such as methylene blue, etc    -   Agents blocking tau aggregation seeding and propagation such as        tau antibodies and tau vaccines, etc    -   Microtubule stabilizers such as AL-108, AL-208, paclitaxel, etc    -   Amyloid-β (A β) peptide lowering agents such as β-secretase        (BACE-1) inhibitors, senile plaque-clearing biologics such as Aβ        antibodies and Aβ vaccines

The invention also relates to a set (kit) consisting of separate packsof an effective amount of a compound according to the invention and/orpharmaceutically acceptable salts, derivatives, solvates andstereoisomers thereof, including mixtures thereof in all ratios, and aneffective amount of a further medicament active ingredient. The setcomprises suitable containers, such as boxes, individual bottles, bagsor ampoules. The set may, for example, comprise separate ampoules, eachcontaining an effective amount of a compound according to the inventionand/or pharmaceutically acceptable salts, derivatives, solvates andstereoisomers thereof, including mixtures thereof in all ratios, and aneffective amount of a further medicament active ingredient in dissolvedor lyophilized form.

Pharmaceutical formulations can be adapted for administration via anydesired suitable method, for example by oral (including buccal orsublingual), rectal, nasal, topical (including buccal, sublingual ortransdermal), vaginal or parenteral (including subcutaneous,intramuscular, intravenous or intra-dermal) methods. Such formulationscan be prepared using processes known in the pharmaceutical art by,e.g., combining the active ingredient with the excipient(s) oradjuvant(s).

The pharmaceutical composition of the invention is produced in a knownway using common solid or liquid carriers, diluents and/or additives andusual adjuvants for pharmaceutical engineering and with an appropriatedosage. The amount of excipient material that is combined with theactive ingredient to produce a single dosage form varies depending uponthe host treated and the particular mode of administration. Suitableexcipients include organic or inorganic substances that are suitable forthe different routes of administration, such as enteral (e.g. oral),parenteral or topical application, and which do not react with compoundsof formula (I′) or (I) or salts thereof. Examples of suitable excipientsare water, vegetable oils, benzyl alcohols, alkylene glycols,polyethylene glycols, glycerol triacetate, gelatin, carbohydrates, e.g.lactose or starch, magnesium stearate, talc and petroleum jelly.

Pharmaceutical formulations adapted for oral administration can beadministered as separate units, such as, for example, capsules ortablets; powders or granules; solutions or suspensions in aqueous ornon-aqueous liquids; edible foams or foam foods; or oil-in-water liquidemulsions or water-in-oil liquid emulsions.

Pharmaceutical formulations adapted for parenteral administrationinclude aqueous and non-aqueous sterile injection solutions comprisingantioxidants, buffers, bacteriostatics and solutes, by means of whichthe formulation is rendered isotonic with the blood of the recipient tobe treated; and aqueous and non-aqueous sterile suspensions, which maycomprise suspension media and thickeners. The formulations can beadministered in single-dose or multi-dose containers, for example sealedampoules and vials, and stored in freeze-dried (lyophilized) state, sothat only the addition of the sterile carrier liquid, for example waterfor injection purposes, immediately before use is necessary. Injectionsolutions and suspensions prepared in accordance with the recipe can beprepared from sterile powders, granules and tablets.

It goes without saying that, in addition to the above particularlymentioned constituents, the formulations may also comprise other agentsusual in the art with respect to the particular type of formulation;thus, for example, formulations which are suitable for oraladministration may comprise flavors.

In a preferred embodiment of the present invention, the pharmaceuticalcomposition is adapted for oral administration. The preparations can besterilized and/or can comprise auxiliaries, such as carrier proteins(e.g. serum albumin), lubricants, preservatives, stabilizers, fillers,chelating agents, antioxidants, solvents, bonding agents, suspendingagents, wetting agents, emulsifiers, salts (for influencing the osmoticpressure), buffer substances, colorants, flavorings and one or morefurther active substances, for example one or more vitamins. Additivesare well known in the art, and they are used in a variety offormulations.

Accordingly, the invention also relates to a pharmaceutical compositioncomprising as active ingredient an effective amount of at least onecompound of formula (I′) or (I) according to the invention and/orphysiologically acceptable salts thereof together with pharmaceuticallytolerable adjuvants for oral administration, optionally in combinationwith at least another active pharmaceutical ingredient. The priorteaching of the present specification concerning administration routeand combination product, respectively, is valid and applicable withoutrestrictions to the combination of both features if expedient.

The terms “effective amount” or “effective dose” or “dose” areinterchangeably used herein and denote an amount of the pharmaceuticalcompound having a prophylactically or therapeutically relevant effect ona disease or pathological conditions, i.e. which causes in a tissue,system, animal or human a biological or medical response which is soughtor desired, for example, by a researcher or physician. A “prophylacticeffect” reduces the likelihood of developing a disease or even preventsthe onset of a disease. A “therapeutically relevant effect” relieves tosome extent one or more symptoms of a disease or returns to normalityeither partially or completely one or more physiological or biochemicalparameters associated with or causative of the disease or pathologicalconditions. In addition, the expression “therapeutically effectiveamount” denotes an amount which, compared with a corresponding subjectwho has not received this amount, has the following consequence:improved treatment, healing, prevention or elimination of a disease,syndrome, condition, complaint, disorder or side-effects or also thereduction in the advance of a disease, complaint or disorder. Theexpression “therapeutically effective amount” also encompasses theamounts which are effective for increasing normal physiologicalfunction.

The respective dose or dosage range for administering the pharmaceuticalcomposition according to the invention is sufficiently high in order toachieve the desired prophylactic or therapeutic effect of reducingsymptoms of the aforementioned diseases. It will be understood that thespecific dose level, frequency and period of administration to anyparticular human will depend upon a variety of factors including theactivity of the specific compound employed, the age, body weight,general state of health, gender, diet, time and route of administration,rate of excretion, drug combination and the severity of the particulardisease to which the specific therapy is applied. Using well-known meansand methods, the exact dose can be determined by one of skill in the artas a matter of routine experimentation. The prior teaching of thepresent specification is valid and applicable without restrictions tothe pharmaceutical composition comprising the compounds of formula (I′)or (I) if expedient.

Pharmaceutical formulations can be administered in the form of dosageunits which comprise a predetermined amount of active ingredient perdosage unit. The concentration of the prophylactically ortherapeutically active ingredient in the formulation may vary from about0.1 to 100 wt %. Preferably, the compound of formula (I′) or (I) or thepharmaceutically acceptable salts thereof are administered in doses ofapproximately 0.5 to 1000 mg, more preferably between 1 and 700 mg, mostpreferably 5 and 100 mg per dose unit. Generally, such a dose range isappropriate for total daily incorporation. In other terms, the dailydose is preferably between approximately 0.02 and 100 mg/kg of bodyweight. The specific dose for each patient depends, however, on a widevariety of factors as already described in the present specification(e.g. depending on the condition treated, the method of administrationand the age, weight and condition of the patient). Preferred dosage unitformulations are those which comprise a daily dose or part-dose, asindicated above, or a corresponding fraction thereof of an activeingredient. Furthermore, pharmaceutical formulations of this type can beprepared using a process which is generally known in the pharmaceuticalart.

Although a therapeutically effective amount of a compound according tothe invention has to be ultimately determined by the treating doctor orvet by considering a number of factors (e.g. the age and weight of theanimal, the precise condition that requires treatment, severity ofcondition, the nature of the formulation and the method ofadministration), an effective amount of a compound according to theinvention for the treatment of neurodegenerative diseases, for exampletauopathies and Alzheimer's disease, is generally in the range from 0.1to 100 mg/kg of body weight of the recipient (mammal) per day andparticularly typically in the range from 1 to 10 mg/kg of body weightper day. Thus, the actual amount per day for an adult mammal weighing 70kg is usually between 70 and 700 mg, where this amount can beadministered as a single dose per day or usually in a series ofpart-doses (such as, for example, two, three, four, five or six) perday, so that the total daily dose is the same. An effective amount of asalt or solvate or of a physiologically functional derivative thereofcan be determined as the fraction of the effective amount of thecompound according to the invention per se. It can be assumed thatsimilar doses are suitable for the treatment of other conditionsmentioned above.

The pharmaceutical composition of the invention can be employed asmedicament in human and veterinary medicine. According to the invention,the compounds of formula (I′) or (I) and/or physiologically saltsthereof are suited for the prophylactic or therapeutic treatment and/ormonitoring of diseases that are caused, mediated and/or propagated byOGA activity. It is particularly preferred that the diseases areneurodegenerative diseases, diabetes, cancer, cardiovascular diseasesand stroke, more preferably neurodegenerative diseases, most preferablyone or more tauopathies, highly preferably Alzheimer's disease anddementia. It shall be understood that the host of the compound isincluded in the present scope of protection according to the presentinvention.

Another aspect of the present invention relates to compounds of formula(I′) or (I) according to the invention and/or physiologically acceptablesalts thereof for use in the prophylactic or therapeutic treatmentand/or monitoring of diseases that are caused, mediated and/orpropagated by OGA activity. Another aspect of the invention concernscompounds of formula (I′) or (I) according to the invention and/orphysiologically acceptable salts thereof for use in the prophylactic ortherapeutic treatment and/or monitoring of neurodegenerative diseases,diabetes, cancer, cardiovascular diseases and stroke. The prior teachingof the present specification concerning the compounds of formula (I) or(I), including any preferred embodiment thereof, is valid and applicablewithout restrictions to the compounds according to formula (I) or (I)and their salts for use in the prophylactic or therapeutic treatmentand/or monitoring of neurodegenerative diseases, diabetes, cancer,cardiovascular diseases and stroke.

Another aspect of the invention relates to a method for treating adisease that is caused, mediated and/or propagated by OGA activity,wherein an effective amount of at least one compound of formula (I′) or(I) according to the invention and/or physiologically acceptable saltsthereof is administered to a mammal in need of such treatment. Anotheraspect of the invention relates to a method for treatingneurodegenerative diseases, diabetes, cancer, cardiovascular diseasesand stroke, preferably a tauopathy, wherein an effective amount of atleast one compound of formula (I′) or (I) according to the inventionand/or physiologically acceptable salts thereof is administered to amammal in need of such treatment. The preferred treatment is an oraladministration. The prior teaching of the invention and its embodimentsis valid and applicable without restrictions to the methods of treatmentif expedient.

The neurodegenerative disease or condition is more preferably selectedfrom the group of one or more tauopathies and Alzheimer's disease,Amyotrophic lateral sclerosis (ALS), Amyotrophic lateral sclerosis withcognitive impairment (ALSci), Argyrophilic grain disease, Behaviorvariant frontotemporal dementia (bvFTD), Bluit disease, Corticobasaldegeneration (CBP), Dementia pugilistica, Dementia with Lewy Bodies,Diffuse neurofibrillary tangles with calcification, Down's syndrome,Familial British dementia, Familial Danish dementia, Frontotemporaldementia with parkinsonism linked to chromosome 17 (FTDP-17),Frontotemporal Lobar Degeneration (FTLD), Ganglioglioma, Gangliocytoma,Gerstmann-Straussler-Scheinker disease, Globular glial tauopathy,Guadeloupean parkinsonism, Hallevorden-Spatz disease (neurodegenerationwith brain iron accumulation type 1), Lead encephalopathy,Lipofuscinosis, Meningioangiomatosis, Multiple system atrophy, Myotonicdystrophy, Niemann-Pick disease (type C), Pallido-ponto-nigraldegeneration, Parkinson's disease, Parkinson's disease dementia (PDD),Parkinsonism-dementia complex of Guam, Pick's disease (PiD),Postencephalitic parkinsonism (PEP), Primary progressive aphasia, Priondiseases (including Creutzfeldt-Jakob Disease (GJD), VariantCreutzfeldt-Jakob Disease (vCJD), Fatal Familial Insomnia, Kuru,Progressive supercortical gliosis, Progressive supranuclear palsy (PSP),Pure Autonomic Failure, Richardson's syndrome, Subacute sclerosingpanencephalitis, Tangle-only dementia, Tuberous Sclerosis, Huntington'sdisease. Most preferred are one ore more tauopathies and Alzheimer'sdisease.

The invention also relates to the use of compounds according to formula(I′) or (I) and/or physiologically acceptable salts thereof for theprophylactic or therapeutic treatment and/or monitoring of diseases thatare caused, mediated and/or propagated by OGA activity. Furthermore, theinvention relates to the use of compounds according to formula (I′) or(I) and/or physiologically acceptable salts thereof for the productionof a medicament for the prophylactic or therapeutic treatment and/ormonitoring of diseases that are caused, mediated and/or propagated byOGA activity. Compounds of formula (I′) or (I) and/or a physiologicallyacceptable salt thereof can furthermore be employed as intermediate forthe preparation of further medicament active ingredients. The medicamentis preferably prepared in a non-chemical manner, e.g. by combining theactive ingredient with at least one solid, fluid and/or semi-fluidcarrier or excipient, and optionally in conjunction with a single ormore other active substances in an appropriate dosage form.

The compounds of formula (I′) or (I) according to the invention can beadministered before or following an onset of disease once or severaltimes acting as therapy. The aforementioned compounds and medicalproducts of the inventive use are particularly used for the therapeutictreatment. A therapeutically relevant effect relieves to some extent oneor more symptoms of a disorder, or returns to normality, eitherpartially or completely, one or more physiological or biochemicalparameters associated with or causative of a disease or pathologicalcondition. Monitoring is considered as a kind of treatment provided thatthe compounds are administered in distinct intervals, e.g. in order tobooster the response and eradicate the pathogens and/or symptoms of thedisease completely. Either the identical compound or different compoundscan be applied. The medicament can also be used to reducing thelikelihood of developing a disorder or even prevent the initiation ofdisorders associated with OGA activity in advance or to treat thearising and continuing symptoms. The disorders as concerned by theinvention are preferably neurodegenerative diseases, diabetes, cancer,cardiovascular diseases and stroke.

In the meaning of the invention, prophylactic treatment is advisable ifthe subject possesses any preconditions for the aforementionedphysiological or pathological conditions, such as a familialdisposition, a genetic defect, or a previously passed disease.

In the scope of the present invention, compounds of formula (I′) or (I)are provided for the first time. The low molecular weight compounds ofthe invention are strong and selective glycosidase inhibitors withimproved passive permeability. The compounds of formula (I′) or (I) havebeen shown to be competitive with PUGNAc, a known OGA inhibitor thatbinds in the substrate pocket. The endogenous substrate is anO-GlcNAcylated protein. O-GlcNAcylation of nuclear and cyto-plasmicproteins is one of the most common post-translational modifications inanimals and plants. O-GlcNAc cycling modulates a number of cellularprocesses, and evidence is mounting that dysregulation ofO-GlcNAcylation plays a role in the etiology of several diseases,including tauopathies and Alzheimer's disease. O-GlcNAc transferase(OGT) and O-GlcNAcase (OGA) are the two enzymes that regulate O-GlcNAccycling. Emerging data suggest that inhibitors that block OGA may helpmaintain healthy O-GlcNAc levels in tauopathies and Alzheimer's diseasepatients and thereby inhibit the formation of neurofibrillary tangles.Hence, the current invention comprises the use of compounds of formula(I′) or (I) in the regulation, modulation and/or inhibition of theglycosidase signal cascade, which can be advantageously applied asresearch tool, for diagnosis and/or in treatment of any disorders thatare responsive to OGA signaling and inhibition.

The low molecular weight inhibitors can be applied either themselvesand/or in combination with physical measurements for diagnostics oftreatment effectiveness. Medicaments and pharmaceutical compositionscontaining said compounds and the use of said compounds to treatglycosidase-mediated conditions is a promising, novel approach for abroad spectrum of therapies causing a direct and immediate improvementin the state of health, whether in man and animal. The impact is ofspecial benefit to efficiently combat tauopathies and Alzheimer'sdisease, either alone or in combination with other neurodegenerativetreatments.

Due to the surprisingly appreciable inhibitory activity on OGA, alongwith passive permeability, the compounds of the invention can beadvantageously administered at lower doses compared to other less potentor selective inhibitors of prior art while still achieving equivalent oreven superior desired biological effects. In addition, such a dosereduction advantageously leads to less or even no medicinal adverseeffects.

The compounds of formula (I′) or (I), their salts, isomers, tautomers,enantiomeric forms, diastereomers, racemates, derivatives, prodrugsand/or metabolites are characterized by a high specificity andstability, low manufacturing costs and convenient handling. Thesefeatures form the basis for a reproducible action, wherein the lack ofcross-reactivity is included, and for a reliable and safe interactionwith the target structure.

All the references cited herein are incorporated by reference in thedisclosure of the invention hereby.

The techniques that are essential according to the invention aredescribed in detail in the specification. Other techniques which are notdescribed in detail correspond to known standard methods that are wellknown to a person skilled in the art, or the techniques are described inmore detail in cited references, patent applications or standardliterature. Although methods and materials similar or equivalent tothose described herein can be used in the practice or testing of thepresent invention, suitable examples are described below. The followingexamples are provided by way of illustration and not by way oflimitation. Within the examples, standard reagents and buffers that arefree from contaminating activities (whenever practical) are used. Theexamples are particularly to be construed such that they are not limitedto the explicitly demonstrated combinations of features, but theexemplified features may be unrestrictedly combined again provided thatthe technical problem of the invention is solved. Similarly, thefeatures of any claim can be combined with the features of one or moreother claims.

EXPERIMENTAL PART

The compounds according to Formula (I′) or (I) can be prepared fromreadily available starting materials by several synthetic approaches,using both solution-phase and solid-phase chemistry protocols or mixedsolution and solid phase protocols. Examples of synthetic pathways aredescribed below in the examples. All reported yields are non optimizedyields. Unless otherwise stated, compounds of Formula (I′) or (I) andrelated formulae obtained as a racemic mixture can be separated toprovide an enantiomerically enriched mixture or a pure enantiomer.

The commercially available starting materials used in the followingexperimental description were purchased from Aldrich, Sigma, ACROS,ABCR, Combi-Blocks, Matrix, Apollo scientific, Alfa Aesar, etc. unlessotherwise reported.

The HPLC, MS and NMR data provided in the examples described below areobtained as followed: ¹H NMR analyses were carried out using BRUKER NMR,model AV-II and AV-III 400 MHz FT-NMR. Residual signal of deuteratedsolvent was used as internal reference. Chemical shifts (δ) are reportedin ppm in relative to the residual solvent signal (δ=2.50 for ¹H NMR inDMSO-d₆, and 7.26 in CDCl₃). s (singlet), d (doublet), t (triplet), q(quadruplet), br (broad), quint (quintuplet).

LCMS Analysis Condition:

Instrument name: Agilent Technologies 1290 infinity 11.

Method A: Method: A-0.1% TFA in H₂O, B-0.1% TFA in ACN; flow rate: 2.0mL/min; column: XBridge C8 (50×4.6 mm, 3.5 μm), +ve mode

Method B: Method: A-10 mM NH₄HCO₃ in H₂O, B-ACN; flow rate: 1.0 mL/min;column: XBridge C8 (50×4.6 mm, 3.5 μm), +ve mode

Method C: Method: A-0.1% HCOOH in H₂O, B-ACN; flow rate: 1.5 ml/min;column: ZORBAX Eclipse XDB-C18 (50×4.6 mm, 3.5 μm), +ve mode

HPLC Analysis Condition:

Instrument name: Agilent 1200 Series instruments as followed using %with UV detection (maxplot).

Method A: Method: A-0.1% TFA in H₂O, B-0.1% TFA in ACN; flow rate: 2.0mL/min; column: XBridge C8 (50×4.6 mm, 3.5 μm).

Method B: Method: A-10 mM NH₄HCO₃ in H₂O, B-ACN; flow rate: 1.0 mL/min;column: XBridge C8 (50×4.6 mm, 3.5 μm).

Chiral SFC Analysis Condition:

Instrument name: PIC-P20 (analytical)

Ratio between CO₂ and co-solvent is ranging between 50:50 and 90:10

Method A: Mobile Phase: 0.5% isopropylamine in IPA, flow rate: 3 mL/min;column: Chiralcel OJ-H (250×4.6 mm, 5 μm).

Method B: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 3mL/min; column: YMC Cellulose C (250×4.6 mm, 5 μm).

Method C: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 4mL/min; column: Lux A1 (250×4.6 mm, 5 μm).

Method D: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 3mL/min; column: Chiralcel OJ-H (250×4.6 mm, 5 μm).

Method G: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 3mL/min; column: Chiralcel OD-H (250×4.6 mm, 5 μm).

Prep-HPLC Condition:

Method A: A-0.1% TFA in H₂O, B-MeOH or CAN; column: Sunfire C8 (19×250mm, 5 μm) or Sunfire C18 (30×250 mm, 10 μm).

Method B: A-10 mM NH₄HCO₃ in H₂O, B-MeOH or ACN, Column: Sunfire C8(19×250 mm, 5 μm) or Sunfire C18 (30×250 mm, 10 μm).

Chiral Preparative SFC Condition:

Instrument name: PIC SFC 100

Ratio between CO₂ and co-solvent is ranging between 50:50 and 90:10

Method A: Mobile Phase: 0.5% isopropylamine in IPA, flow rate: 100mL/min; column: Chiralcel OJ-H (250×30 mm, 5 μm).

Method B: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 100mL/min; column: YMC Cellulose C (250×30 mm, 5 μm).

Method C: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 100mL/min; column: Lux A1 (250×30 mm, 5 μm).

Method D: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 100mL/min; column: Chiralcel OJ-H (250×30 mm, 5 μm).

Method E: Mobile Phase: 0.5% isopropylamine in IPA, flow rate: 100mL/min; column: YMC Amylose SA (250×30 mm, 5 μm).

Method F: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 100mL/min; column: YMC Amylose SA (250×30 mm, 5 μm).

Method G: Mobile Phase: 0.5% isopropylamine in methanol, flow rate: 100mL/min; column: Chiralcel OD-H (250×30 mm, 5 μm).

General flash chromatography conditions used for the purification ofintermediates or compounds of Formula I: silica gel 230-400 mesh;gradients used as elutent: 10 to 80% EtOAc in petroleum ether or 1 to15% MeOH in DCM.

The microwave chemistry was performed on a single mode microwave reactorInitiator™ Sixty from Biotage.

Specific Optical Rotation

Instrument name: Autopol VI, by Rudolph Research Analytical,Hackettstown, N.J., USA.

Intermediate 1: 5-(1-chloroethyl)benzo[c][1,2,5]thiadiazole

Step 1: 1-(benzo[c][1,2,5]thiadiazol-5-yl)ethan-1-ol

A stirred solution of benzo[c][1,2,5]thiadiazole-5-carbaldehyde (1.0 g,6.10 mmol) in dry THF (10 mL) under nitrogen atmosphere was cooled in anice bath, followed by the slow addition of methylmagnesium chloride (3.0mL, 9.13 mmol, 3 M in THF) and the reaction mixture was stirred for 2 hat the same temperature. Upon completion (TLC), the reaction mixture wasquenched with aq. sat. NH₄Cl solution and extracted with ethyl acetate.The combined organic layer was washed with water, brine solution, driedover sodium sulphate (Na₂SO₄) and evaporated under reduced pressure. Theresulting crude was purified by flash chromatography (Silica gel:230-400 mesh, Eluent: 25% ethyl acetate in petroleum ether) to give thetitle compound. Yield: 55% (600 mg, pale orange solid). ¹H NMR (400 MHz,DMSO-d₆): δ 8.12-7.92 (m, 2H), 7.66 (dd, J=2.0, 9.0 Hz, 1H), 5.11 (q,J=6.8 Hz, 1H), 1.61 (dd, J=6.4 Hz, 3H). LCMS: (Method A) 181.0 (M+H),Rt. 2.0 min, 97.1% (Max).

Step 2: 5-(1-chloroethyl)benzo[c][1,2,5]thiadiazole

To a stirred solution of Step 1: Intermediate 1, (0.5 g, 2.77 mmol) indry DCM (4 mL) was added thionyl chloride (0.3 mL, 4.13 mmol) slowly at0° C. The reaction mixture was stirred at RT for 1 h. The reactionmixture was concentrated under vacuum and co-distilled with DCM (3×5mL). Then completely dried under vacuum to give the title compound whichwas used in the next step without further purification. Yield: 90% (500mg, pale orange gum). LCMS: (Method A) 163.1 (M−HCl), Rt. 2.9 min, 76.0%(Max).

Intermediate 2: 5-(1-chloroethyl)benzo[d]thiazole

Step 1: 1-(benzo[d]thiazol-5-yl)ethan-1-one

To a degassed solution of 5-bromo benzothiazole (750 g, 3.51 mol) in drytoluene (6 L), 1-ethoxyvinyl tributyltin (1.42 L, 4.21 mol) followed byPd(PPh₃)₂Cl₂ (105.6 g, 150.7 mmol) were added at RT and the resultingmixture was heated at 90° C. for 16 h. After completion of the reaction(monitored by TLC), the reaction mixture was cooled to RT, filteredthrough celite and washed with EtOAc (1 L). The filtrate was evaporatedunder vacuum and 5N HCl solution (2.5 L) was added to the crude mixture.The resulting light brown coloured solution was stirred at RT for 1.5 h,neutralized with the slow addition of a saturated NaHCO₃ solution (12 L)over 1 h at 0° C. and was extracted with EtOAc (2×5 L). The combinedorganic layer was washed with brine solution (2.5 L), dried overanhydrous Na₂SO₄ and evaporated under vacuum. The resulting crudematerial was dissolved in DCM (750 mL), hexane (3 L) was added to it andthe resulting solid was filtered. The solids were washed with MTBE (4L). The combined filtrate was concentrated under vacuum. The residue wasdissolved in EtOAc (2.5 L) and charcoal (35 g) was added. The organiclayer was stirred for 6 h at RT and filtered and solids were washed withexcess of EtOAc (1 L). The organic layer was concentrated to afford thetitle compound. Yield: 79% (475 g, light brown solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.53 (s, 1H), 8.69 (s, 1H), 8.32 (d, J=8.4 Hz, 1H), 8.04(dd, J=8.4, 1.3 Hz, 1H), 2.71 (s, 3H). LCMS: (Method C) 178.0 (M+H), Rt.1.4 min, 98.5% (Max). HPLC: (Method A) Rt 2.6 min, 97.2% (Max).

Step 2: 1-(benzo[d]thiazol-5-yl)ethan-1-ol

To a stirred solution of 1-(benzo[d]thiazol-5-yl)ethan-1-one (475 g,2.68 mol)) in methanol (4.75 L), NaBH₄ (152.28 g, 4.03 mol) was addedportion wise at 0° C. and the reaction mixture was stirred at RT for 1h. Completion of the reaction was monitored by TLC, the reaction mixturewas then quenched with ice water (400 mL) at 0° C. and concentratedunder vacuum. To the resulting crude mixture, water (2.5 L) was addedand the aqueous layer was extracted with EtOAc (2×2.5 L). The combinedorganic layer was washed with brine (2 L), dried over anhydrous Na₂SO₄and concentrated under vacuum. The resulting crude solid was trituratedwith hexane:diethyl ether (8:2) and decanted to afford the titlecompound. Yield: 93% crude (440 g, pale brown gummy solid). ¹H NMR (400MHz, DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.04 (s, 1H),7.50 (d, J=1.2 Hz, 1H), 5.32 (d, J=4.0 Hz, 1H), 4.93-4.89 (m, 1H), 1.40(d, J=6.4 Hz, 3H). LCMS: (Method C) 180.1 (M+H), Rt. 1.2 min, 98.7%(Max). HPLC: (Method A) Rt. 2.2 min, 99.5% (Max).

Step 3: 5-(1-chloroethyl)benzo[d]thiazole

To a stirred solution of 1-(benzo[d]thiazol-5-yl)ethan-1-ol (440 g, 2.46mol)) in DCM (4.4 L), thionyl chloride (534 mL, 7.37 mol) was added dropwise over 30 min at 0° C. and the reaction mixture was stirred for 1 hat 0-10° C. Completion of the reaction was monitored by TLC, thereaction mixture was then evaporated under vacuum. The resulting crudematerial was co-distilled with dry DCM (3×400 mL), dried under vacuum toafford title compound which was used in the next step without furtherpurification. Yield: 100% crude (488 g, yellow solid). ¹H NMR (400 MHz,DMSO-d₆): δ 10.79 (s, 1H), 8.52 (s, 1H), 8.16 (d, J=8.4 Hz, 1H), 7.86(d, J=8.4 Hz, 1H), 5.30-5.24 (m, 1H), 1.91 (d, J=6.8 Hz, 3H). LCMS:(Method C) 198.1 (M+H), Rt. 2.0 min, 50.1% (Max). HPLC: (Method A) Rt.3.9 min, 66.8% (Max).

Intermediate 3: 6-(1-chloroethyl)-2, 3-dihydrobenzofuran

Step 1: 2-(2, 5-dibromophenoxy)ethan-1-ol

To a stirred solution of 1, 4-dibromo-2-fluorobenzene (Combi-Blocks,1000 g, 3.94 mol) in ethylene glycol (5100 mL), NMP (500 mL) was addedat RT under nitrogen atmosphere. Then KO^(t)Bu (1547 g, 1.38 mol) wasadded in portions over 45 min at 5° C. and the resulting mixture washeated at 90° C. for 16 h. Completion of the reaction was monitored byHPLC (Method A), the reaction mixture was then cooled to RT. dilutedwith water (2000 mL) and stirred for 15 min. The resulting solid wasfiltered and washed with ethylene glycol (2×300 mL). Water (16000 mL)was added to the filtrate, cooled to 10° C. and stirred for 1 h at thesame temperature to precipitate out the whole solid. The obtained solidwas filtered and washed with water (2×1000 mL), petroleum ether (3×1000mL) and dried under vacuum. This solid was co-distilled with toluene(3×500 mL) to afford the title compound. Yield: 78% (910 g, whitesolid). ¹H NMR (400 MHz, CDCl₃): δ 7.41 (d, J=8.0 Hz, 1H), 7.06-7.00 (m,2H), 4.14 (t, J=4.0 Hz, 2H), 4.01 (q, J=3.6 Hz, 2H). LCMS: (Method A)296.0 (M+H), Rt. 3.9 min, 98.2% (Max). HPLC: (Method A) Rt. 3.7 min,99.5% (Max).

Step 2: 1, 4-dibromo-2-(2-bromoethoxy)benzene

To a stirred solution of 2-(2, 5-dibromophenoxy) ethan-1-ol (910.0 g,3.07 mol) in toluene (6370 mL), PBr₃ (Aldrich, 145 mL, 1.54 mol) wasadded under nitrogen atmosphere at 0° C. over 15 min. The resultingmixture was heated at 90° C. for 4 h and then cooled to 0° C. PBr₃(13.57 mL, 142.92 mmol) was added followed by the slow addition of water(20 mL) and heating was continued at 90° C. for 3 h. Completion of thereaction was monitored by TLC, the reaction mixture was then cooled to10° C. and quenched with NaOH solution (1 N, 2200 mL). The milky solidlayer, formed immediately after quenching, was filtered through celitepad. The organic layer was separated, washed with water (1820 mL), brinesolution (1820 mL) and dried over anhydrous Na₂SO₄. It was thenevaporated at 45° C. under vacuum. The resulting crude material wasdissolved in EtOAc (3185 mL), the organic layer was washed with water(1820 mL), brine solution (1820 mL) and dried over anhydrous Na₂SO₄. Theorganic layer was evaporated at 40° C. under reduced pressure to affordthe title compound. Yield: 86% (946 g, white solid). ¹H NMR (400 MHz,DMSO-d₆): δ 7.54 (d, J=8.4 Hz, 1H), 7.36 (d, J=1.6 Hz, 1H), 7.13-7.10(m, 1H), 4.45 (t, J=1.2 Hz, 2H), 3.82 (t, J=1.6 Hz, 2H). HPLC: (MethodA) Rt. 4.7 min, 93.0% (Max).

Step 3: 2, 3-dihydrobenzofuran-6-carbaldehyde

To a stirred solution of 1, 4-dibromo-2-(2-bromoethoxy)benzene (946 g,2.64 mol) in dry THF (9.5 L) under nitrogen atmosphere, n-butyl lithium(1812 mL, 2.89 mol, 1.6 M in hexane) was added slowly over 30 min at−78° C. and stirring was continued for 1 h at the same temperature. Asecond batch of n-butyl lithium (1812 mL, 2.89 mol, 1.6 M in hexane) wasadded slowly over 30 min at −78° C. and stirring was continued foranother 1 h. Then DMF (408 mL, 5.27 mol) was added slowly at sametemperature and the mixture was stirred for 45 min. After completion ofthe reaction (monitored by TLC), the reaction mixture was warmed to 10°C., quenched with the addition of sat. NH₄Cl solution (3784 mL) and theaqueous layer was extracted with EtOAc (2×2800 mL). The combined organiclayer was washed with water (2838 mL), brine solution (2838 mL), driedover anhydrous Na₂SO₄ and evaporated at 40° C. under reduced pressure toafford the title compound. Yield: 96% crude (404 g, pale brown gummysolid). ¹H NMR (400 MHz, DMSO-d₆): δ 9.90 (s, 1H), 7.45 (dd, J=5.2, 1.2Hz, 2H), 7.19 (s, 1H), 4.60 (t, J=8.7 Hz, 2H), 3.27 (t, J=8.7 Hz, 2H).HPLC: (Method A) Rt. 2.9 min, 84.3% (Max).

Step 4: 1-(2, 3-dihydrobenzofuran-6-yl)ethan-1-ol

To a stirred solution of 2, 3-dihydrobenzofuran-6-carbaldehyde (404 g,2.73 mol) in dry THF (4040 mL) under nitrogen atmosphere, methylmagnesium chloride solution (1820 mL, 5.45 mol, 3 M in THF) was addedslowly over 30 min at 0° C. and stirred for 2 h at RT. Completion of thereaction was monitored by TLC, the reaction mixture was then quenched byusing sat. NH₄Cl solution (1616 mL) and extracted with EtOAc (2×2828mL). The combined organic layer was washed with water (1616 mL), brinesolution (1616 mL), dried over Na₂SO₄ and evaporated at 45° C. underreduced pressure. The resulting crude material was purified by flashchromatography (silica gel: 60-120 mesh, eluent: 18% EtOAc in petroleumether) to afford the title compound. Yield: 46% (210 g, pale brown gummysolid). ¹H NMR (400 MHz, DMSO-d₆): δ 7.12 (d, J=7.2 Hz, 1H), 6.77 (dd,J=7.6, 0.8 Hz, 1H), 6.72 (s, 1H), 5.05 (d, J=4.4 Hz, 1H), 4.66-4.60 (m,1H), 4.48 (t, J=8.4 Hz, 2H), 3.12 (t, J=8.4 Hz, 2H), 1.28 (t, J=6.8 Hz,3H). LCMS: (Method A) 147.0 (M−H₂O+H), Rt. 2.7 min, 90.7% (Max). HPLC:(Method A) Rt. 2.6 min, 91.7% (Max).

Step 5: 6-(1-chloroethyl)-2, 3-dihydrobenzofuran

To a stirred solution of 1-(2, 3-dihydrobenzofuran-6-yl)ethan-1-ol (200g, 1.22 mmol) in DCM (1600 mL) at 0° C., oxalyl chloride (155 mL, 3.66mmol) and catalytic amount of DMF (2 mL) were added and the reactionmixture was stirred at RT for 16 h. Then the reaction mixture wasconcentrated under vacuum and co-distilled with dry DCM (3×500 mL) toafford the title compound. Yield: 97% (crude) (220 g, pale brown gummysolid). ¹H NMR (400 MHz, DMSO-d₆): δ 7.32 (d, J=7.6 Hz, 1H), 6.92 (d,J=9.6 Hz, 2H), 5.28 (q, J=13.2 Hz, 1H), 4.52 (t, J=8.4 Hz, 2H), 3.15 (t,J=8.8 Hz, 2H), 1.75 (d, J=8.4 Hz, 3H). LCMS: (Method A) 147.2 (M+H-HCl),Rt. 4.2 min, 77.2% (Max).

Intermediate 4: 6-(1-chloroethyl)quinoxaline

Step 1: 1-(quinoxalin-6-yl)ethan-1-one

To a degassed stirred solution of 6-bromo quinoxaline (2.0 g, 9.50 mmol)in toluene (20 mL), 1-ethoxyvinyl tributyltin (3.8 g, 10.5 mmol)followed by Pd(PPh₃)₂Cl₂ (0.67 g, 0.95 mmol) were added at RT and thereaction mixture was stirred at 90° C. overnight. After completion ofthe reaction (monitored by TLC), the reaction mixture was cooled to RT.filtered through celite and the obtained filtrate was evaporated undervacuum. To the resulting crude mixture, 6 N HCl solution (20 mL) wasadded and the reaction mixture was stirred at RT for 1 h. The solutionwas neutralized with sat. NaHCO₃ and the aqueous layer was extractedwith DCM (2×100 mL). The combined organic layer was dried over Na₂SO₄and concentrated under vacuum. The resulting crude material was purifiedby flash chromatography (eluent: 30% EtOAc in hexane) to afford thetitle compound. Yield: 45% (800 mg, brown solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.06-9.04 (m, 2H), 8.70 (d, J=2.4 Hz, 1H), 8.28 (dd, J=8.8,2.8 Hz, 1H), 8.16 (d, J=8.4 Hz, 1H), 2.97 (s, 3H). LCMS: (Method A) 173(M+H), Rt. 2.2 min, 99.1% (Max).

Step 2: 1-(quinoxalin-6-yl)ethan-1-ol

To a stirred solution of 1-(quinoxalin-6-yl)ethan-1-one (0.8 g, 4.65mmol) in dry methanol (20 mL) at 0° C., NaBH₄ (0.36 g, 9.30 mmol) wasadded portion wise and the resulting mixture was stirred for 1 h. Aftercompletion of the reaction (monitored by TLC), the reaction mixture wasquenched with ice-cold water and the aqueous layer was extracted withDCM (2×40 mL). The combined organic layer was washed with water (20 mL),dried over anhydrous Na₂SO₄ and concentrated under vacuum. The resultingcrude material was forwarded to the next step without any furtherpurification. Yield: 75% (600 mg, dark brown liquid). ¹H NMR (400 MHz,DMSO-d₆): δ 8.91-8.89 (m, 2H), 8.03 (t, J=11.6 Hz, 2H), 7.87-7.86 (m,1H), 5.49 (d, J=5.9 Hz, 1H), 4.98-4.97 (m, 1H), 1.42 (d, J=8.6 Hz, 3H).LCMS: (Method A) 175.0 (M+H), Rt. 1.89 min, 95.0% (Max).

Step 3: 6-(1-chloroethyl)quinoxaline

To a stirred solution of 1-(quinoxalin-6-yl)ethan-1-ol (0.6 g, 3.46mmol) in dry DCM (10 mL), thionyl chloride (0.5 mL, 6.93 mmol) was addeddropwise at 0° C. and stirred at RT for 1 h. The reaction mixture wasevaporated to dryness under vacuum and the resulting crude material wasforwarded to the next step as such without any further purification.Yield: 97% (650 mg, off white solid). ¹H NMR (400 MHz, DMSO-d₆): δ 8.74(s, 2H), 7.93 (s, 1H), 7.70-7.68 (m, 2H), 4.46-4.23 (m, 1H), 1.87 (s,3H). LCMS: (Method A) 193.0 (M+H), Rt. 3.4 min, 71.4% (Max).

Intermediate 5: tert-butyl7-bromo-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate andtert-butyl 7-bromo-1,3,4,5-tetrahydro-2H-benzo[c]azepine-2-carboxylate

Step 1: 7-bromo-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one and7-bromo-1,2,4,5-tetrahydro3H-benzo[c]azepin-3-one

To a stirred solution of 6-bromo-3,4-dihydronaphthalen-2(1H)-one (1.0 g,11.1 mmol) in MeSO₃H (10 mL), was added NaN₃ (1.58 g, 12.3 mmol) slowly,in portions at 0° C. The reaction mixture was stirred at RT for 2 h.After completion (by TLC), all the batches were combined and slowlyadded to ice cooled KOH (1 M) solution. The resulting mixture wasextracted with EtOAc (2×50 mL), and the combined organic layer was driedover Na₂SO₄ and concentrated. Five batches of this reaction wereperformed and the combined crude material was purified by flashchromatography using 1-2% MeOH in DCM to afford mixture of tittlecompound as a mixture of regioisomers. Yield: 62% (3.25 g, dark brownsolid). LCMS: (Method A) 241.9 (M+H), Rt. 2.2 min, 74.6% (Max).

Step 2: 7-bromo-2,3,4,5-tetrahydro-1H-benzo[d]azepine and7-bromo-2,3,4,5-tetrahydro-1H-benzo[c]azepine

To a stirred solution of Step 1: Intermediate 5 (3.25 g, 13.43 mmol) inTHF (30 mL) was added a solution of BH₃-THF (1.0 M, 21 mL, 21 mmol) at0° C. and the mixture was stirred at 65° C. for overnight. Completion ofthe reaction was monitored by TLC. After completion, the reactionmixture was slowly quenched with methanol (21 mL) at 0° C. and thenheated to 50° C. for 1 h. Then reaction mixture was concentrated underreduced pressure. The residue was as such taken for next step withoutany purification. Yield: 42% (2.2 g, pale brown gummy solid). LCMS:(Method A) 227.9 (M+H), Rt. 1.9 min, 48.6% (Max).

Step 3: tert-butyl7-bromo-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate andtert-butyl7-bromo-1,3,4,5-tetrahydro-2H-benzo[c]azepine-2-carboxylate

To a stirred solution of Step 2: Intermediate 5 (2.2 g, 9.69 mmol) andTEA (3.4 mL, 24.44 mmol) in DCM (3 mL), was added (Boc)₂O (3.1 g, 14.6mmol) at 0° C. and the mixture was stirred at RT for overnight.Completion of the reaction was monitored by TLC and the reaction mixturewas evaporated at 50° C. under reduced pressure. The resulting crude waspurified by flash chromatography using 1-2% MeOH in DCM to afford thetittle compound. Yield: 76% (2.4 g, pale brown gummy solid). LCMS:(Method A) 227.9 (M-Boc), Rt. 3.3 min, 78.1% (Max).

Intermediate 6: 7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Step 1: N-(2,2-dimethoxyethyl)-2-(4-methoxyphenyl)acetamide

To a stirred solution of 2-(4-methoxyphenyl)acetic acid (5.0 g, 30.08mmol) in DCM (50 mL), were added aminoacetaldehyde (3.79 g, 36.10 mmol),TEA (12.5 mL, 90.25 mmol), T3P (28.7 mL, 45.12 mmol) and the reactionmixture was stirred at RT for overnight. The completion of the reactionwas confirmed by TLC. The reaction mixture was quenched with water (100mL), extracted with DCM (2×150 mL), washed with aq. NaHCO₃ solution(10%, 100 mL) and brine (50 mL). The organic layer was dried over Na₂SO₄and concentrated. The crude material was purified by flashchromatography using 50-60% EtOAc in petroleum ether to afford the titlecompound. Yield: 70% (5.3 g, pale yellow gum). ¹H NMR (400 MHz,DMSO-d₆): δ 8.18-8.10 (m, 1H), 7.22-7.19 (m, 1H), 6.83-6.77 (m, 3H),4.33 (t, J=8.4 Hz, 1H), 3.73 (s, 3H), 3.33 (s, 2H), 3.25 (s, 6H),3.17-3.12 (m, 2H). LCMS: (Method D) 254.1 (M+H), Rt. 2.0 min, 98.8(Max).

Step 2: 8-methoxy-1,3-dihydro-2H-benzo[d]azepin-2-one

A solution of N-(2,2-dimethoxyethyl)-2-(4-methoxyphenyl)acetamide (5.3g, 20.91 mmol, Step 1: Intermediate 6) in concentrated HCl (50 mL, 10 V)and glacial acetic acid (53 mL) was stirred at RT overnight. Thecompletion of the reaction was confirmed by TLC, the reaction mixturewas quenched with water (100 mL) and the resulting solid was filtered.It was washed with petroleum ether and dried under vacuum to afford thetitle compound. Yield: 53% (2.1 g, brown solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.50 (s, 1H), 7.20 (d, J=7.6 Hz, 1H), 6.95-6.78 (m, 2H),6.28-6.14 (m, 2H), 3.77 (s, 3H), 3.35 (s, 2H). LCMS: (Method A) 190.0(M+H), Rt. 2.1 min, 98.9% (Max).

Step 3: 8-methoxy-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one

8-methoxy-1,3-dihydro-2H-benzo[d]azepin-2-one (2.1 g, 30.08 mmol, Step2: Intermediate 6) was dissolved in methanol and acetic acid (1:1, mL).Palladium on carbon (10 wt %, 0.2 g) was added to the reaction mixtureand the suspension was put under hydrogen pressure (3 kg/cm²) for at RT8 h. After completion, the catalyst was filtered off through a pad ofcelite, and the filtrate was concentrated to afford the title compoundwhich was used without further purification. Yield: 90% (1.9 g, Brownsolid). LCMS: (Method A) 192.0 (M+H), Rt. 1.6 min, 99.3% (Max).

Step 4: 7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine

To a stirred solution of8-methoxy-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one (1.9 g, 9.93 mmol,Step 3: Intermediate 6) in THF (6 mL) at 0° C. was added a solution ofBH₃-THF (14.9 mL, 1.0 M, 14.9 mmol) and the mixture was stirred at 65°C. for overnight. After completion, the reaction mixture was slowlyquenched with methanol (6 mL) at 0° C. followed by HCl (1.5 N, 6 mL) andthe mixture was heated to 50° C. for 1 h. Then reaction mixture wasconcentrated under reduced pressure and washed with EtOAc (2×50 mL). Theaqueous layer was basified with 10% aq. NaOH to neutral pH and extractedwith EtOAc (2×150 mL). The combined organic layer was dried over Na₂SO₄,filtered and concentrated to afford the tittle compound. Yield: 69% (1.2g, pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆): δ 7.11 (d, J=11.0 Hz,1H), 6.80-6.71 (m, 2H), 3.74 (s, 3H), 3.61 (t, J=9.0 Hz, 2H), 3.44 (t,J=18.2 Hz, 2H), 1.80-1.70 (m, 2H), 1.57-1.45 (m, 2H). LCMS: (Method A)178.1 (M+H), Rt. 1.3 min, 86.1% (Max).

Intermediate 7: tert-butyl7-hydroxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate

Step 1: 2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol

To a stirred solution of 7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.9 g, 5.07 mmol, Intermediate 6) in DCM (9.0 mL),was added BBr₃ (7.6 mL, 1.0 M solution in DCM) at 0□ and the reactionmixture was stirred at RT for overnight. After completion of reaction(TLC), the reaction mixture was quenched by methanol at 0□ andconcentrated under reduced pressure. The resulting solid was trituratedwith hexane-diethyl ether (8:2) to give the title compound. Yield: 75%(0.9 g, brown gum). ¹H NMR (400 MHz, DMSO-d₆): δ 6.98 (d, J=8.0 Hz, 1H),6.62-6.54 (m, 2H), 3.17-3.12 (m, 4H), 2.98-2.95 (m, 4H). LCMS: (MethodA) 164.2 (M+H), Rt. 0.7 min, 69.4% (Max).

Intermediate 7: tert-butyl7-hydroxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate

To a stirred solution of 2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol (0.9g, 5.52 mmol, Step 1: Intermediate 7) in DCM (9.0 mL), were added TEA(2.30 mL, 16.56 mmol) and Boc-anhydride (1.8 mL, 8.27 mmol) at 0□ andthe reaction mixture was stirred at room temperature for overnight.Completion of the reaction was monitored by TLC. After completion ofreaction, the reaction mixture was quenched by water and extracted withEtOAc (2×150 mL). The combined organic layer was dried over Na₂SO₄ andconcentrated to afford the tittle compound. Yield: 76% (1.1 g, whitesolid). ¹H NMR (400 MHz, DMSO-d₆): δ 6.98 (d, J=8.0 Hz, 1H), 6.62-6.54(m, 2H), 3.17-3.12 (m, 4H), 2.98-2.95 (m, 4H), 1.41 (s, 9H). LCMS:(Method A) 164.2 (M+H), Rt. 0.73 min, 69.38% (Max).

Intermediate 8: 7-methoxy-2-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Step 1: methyl (2-(3-methoxyphenyl)acetyl)alaninate

To a stirred solution of 2-(3-methoxyphenyl)acetic acid (5.0 g, 30.30mmol), methyl alaninate hydrochloride (4.63 g, 33.15 mmol) and TEA (10.5mL, 75.38 mmol) added T₃P (50% in EtOAc, 28.7 mL, 45.21 mmol) at 0° C.and stirred at RT for 4 h. Completion of the reaction was monitored byTLC. The reaction mixture was diluted with water (100 mL), extractedwith EtOAc (3×50 mL), and the combined organic layer was dried overNa₂SO₄ and concentrated to give the tittle compound. Yield: 63% (4.7 g,pale brown gummy solid). LCMS: (Method A) 252.0 (M+H), Rt. 2.2 min,90.7% (Max).

Step 2: N-(1-hydroxypropan-2-yl)-2-(3-methoxyphenyl)acetamide

To a stirred solution of Step 1: Intermediate 8, (4.7 g, 18.65 mmol) inMeOH (50 mL), was added NaBH₄ (2.8 g, 74.9 mmol) slowly at 0° C. Thenreaction mixture stirred at RT for overnight. Completion of the reactionwas monitored by TLC. The reaction mixture was diluted with water (50mL), extracted with EtOAc (2×50 mL), and the combined organic layer wasdried over Na₂SO₄ and concentrated. The crude residue obtained waspurified by flash chromatography using 1-2% MeOH in DCM to afford thetittle compound. Yield: 76% (3.2 g, off white solid). ¹H NMR (400 MHz,DMSO-d₆): δ 7.83-7.81 (m, 1H), 7.22-7.17 (m, 1H), 6.82-6.77 (m, 3H),4.70-4.66 (m, 1H), 3.73-3.71 (m, 4H), 3.32 (s, 3H), 3.25-3.19 (m, 1H),1.01 (d, J=8.8 Hz, 3H). LCMS: (Method A) 224.1 (M+H), Rt. 2.0 min, 87.4%(Max).

Step 3: N-(1,1-dimethoxypropan-2-yl)-2-(3-methoxyphenyl)acetamide

To a stirred solution of Step 2: Intermediate 8, (3.2 g, 14.35 mmol) indry DCM (32 mL), was added Dess-Martin periodinane (7.3 g, 17.21 mmol)slowly at 0° C. and the reaction mixture was stirred at 0° C. for 3 h.After completion, the reaction mixture was filtered through a cellitepad and the filtrate was washed with aq. NaHCO₃ solution (50 mL). Theorganic layer was concentrated at 40° C. The resulting residue wasdiluted with MeOH (30 mL). Then trimethyl orthoformate (3 mL, 28.1mmol), and PTSA (0.27 g, 1.4 mmol) were added and the mixture was heatedto 50° C. for 3 h. After completion, the reaction mixture wasconcentrated, the residue was diluted with aq. NaHCO₃ solution (30 mL)and extracted with EtOAc (2×50 mL). The combined organic layer was driedover Na₂SO₄ and concentrated. The crude residue was purified by flashchromatography using 1-2% MeOH in DCM to afford the tittle compound.Yield: 56% (2.1 g, off white solid). ¹H NMR (400 MHz, CDCl₃): δ7.29-7.27 (m, 1H), 6.86-6.83 (m, 3H), 5.65-5.60 (m, 1H), 4.21-4.17 (m,1H), 4.13 (d, J=3.6 Hz, 1H), 3.83 (s, 3H), 3.55 (s, 2H), 3.40 (s, 3H),3.36 (s, 3H), 1.08 (d, J=6.8 Hz, 3H). LCMS: (Method A) 236.1 (M−32), Rt.2.3 min, 83.7% (Max).

Step 4: 8-methoxy-4-methyl-1,3-dihydro-2H-benzo[d]azepin-2-one

To a stirred solution of Step 3: Intermediate 8, (2.1 g, 7.83 mmol) inAcOH (10 mL), was added aq. HCl (36%, 10 mL) slowly at 0° C. and thereaction mixture was stirred at RT for overnight. After completion, thereaction mixture was diluted with water (30 mL), and extracted withEtOAc (2×50 mL). The combined organic layer was dried over Na₂SO₄ andconcentrated to afford the tittle compound. Yield: 51% (0.8 g, off whitesolid). LCMS: (Method A) 204.3 (M+H), Rt. 2.3 min, 56.6% (Max).

Step 5: 8-methoxy-4-methyl-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one

To a stirred solution of Step 4: Intermediate 8 (0.8 g, 3.94 mmol) in(1:1) MeOH—AcOH (20 mL), was added 10% Pd—C (160 mg) at RT and thereaction mixture was stirred at RT for 3 days at 1 kg/cm³ pressure.After completion, the reaction mixture was filtered through a celitepad, and the filtrate was concentrated to get the tittle compound.Yield: 76% (0.6 g, off white solid). LCMS: (Method A) 206.1 (M+H), Rt.1.8 min, 80.6% (Max).

Step 6: 7-methoxy-2-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

To a stirred solution of Step 5: Intermediate 8 (0.6 g, 2.91 mmol) inTHF (6 mL) was added a solution of BH₃-THF (1.0 M, 6 mL, 5.8 mmol) at 0°C. and the mixture was stirred at 65° C. for overnight. Completion ofthe reaction was monitored by TLC. After completion, the reactionmixture was slowly diluted with methanol (6 mL) at 0° C. followed by 1.5N HCl (6 mL) and then the mixture was heated to 50° C. for 1 h. Thereaction mixture was concentrated under reduced pressure and washed withEtOAc (2×20 mL). The aqueous layer was collected and basified with 10%NaOH solution to neutral pH and extracted with EtOAc (2×25 mL). Thecombined organic layer was dried over Na₂SO₄ and concentrated to affordthe tittle compound. Yield: 48% (0.27 g, off white gummy solid). LCMS:(Method A) 192.2 (M+H), Rt. 2.0 min, 63.2% (Max).

Intermediate 9: 6-(1-chloroethyl)-2,3-dihydrofuro[3,2-b]pyridine

Step 1: methyl 5-hydroxy-6-iodonicotinate

To a stirred solution of methyl 5-hydroxynicotinate (10 g, 65.29 mmol)in a mixture of THF (200 mL) and water (200 mL) were added I₂ (41.4 g,163.2 mmol) and Na₂CO₃ (20.7 g, 195.8 mmol) and the stirring wascontinued at RT for 4 h. Completion of the reaction was monitored byTLC. The reaction mixture was quenched with sat. aq. Na₂S₂O₃ and thenneutralized with aq. HCl (6 N). The resulting mixture was extracted withEtOAc (2×200 mL) and the combined organic layer was dried over Na₂SO₄and concentrated to afford the title compound. Yield: 67% (1.5 g, browngum). ¹H NMR (400 MHz, DMSO-d₆): δ 11.42 (s, 1H), 8.33 (d, J=2.0 Hz,1H), 7.54 (d, J=1.6 Hz, 1H), 3.86 (s, 3H). LCMS: (Method A) 280.0 (M+H),Rt. 2.7 min, 92.5% (Max).

Step 2: methyl 5-acetoxy-6-iodonicotinate

To a stirred solution of methyl 5-hydroxy-6-iodonicotinate (12.5 g,65.29 mmol, Step 1: Example 34) in DCM (250 mL) at 0° C. were addedacetyl chloride (41.4 g, 163.2 mmol) and TEA (20.7 g, 195.8 mmol) andthe stirring was continued at RT for 1 h. Upon completion (TLC), thereaction mixture was quenched with aq. sodium bicarbonate solution andthe mixture was extracted with DCM (2×250 mL). The combined organiclayer was dried over Na₂SO₄ and concentrated to afford the titlecompound. Yield: 97% (14.0 g, brown gum). LCMS: (Method A) 322.0 (M+H),Rt. 3.6 min, 79.8% (Max).

Step 3: methyl 5-acetoxy-6-((trimethylsilyl)ethynyl)nicotinate

A stirred solution of methyl 5-acetoxy-6-iodonicotinate (14.0 g, 43.60mmol, Step 2: Example 34) in THF (140 mL) was degassed with N₂ for 10min at RT. TMS-acetylene (7.2 mL, 5.1 g, 52.32 mmol), TEA (18.2 mL,130.84 mmol), CuI (0.83 g, 4.36 mmol) and Pd(PPh₃)₂Cl₂ (1.53 g, 2.18mmol) were added to the reaction mixture and the stirring was continuedovernight at RT. Completion of the reaction was monitored by TLC. Thereaction mixture was filtered through a celite pad and the filtrate wasdiluted with ethyl acetate. The mixture was washed with water (280 mL),brine (120 mL), dried over Na₂SO₄ and concentrated to afford the titlecompound. Yield: 87% (11.1 g, brown gum). LCMS: (Method A) 292.1 (M+H),Rt. 3.6 min, 60.4% (Max).

Step 4: methyl furo[3,2-b]pyridine-6-carboxylate

Potassium fluoride (2.21 g, 38.09 mmol) was added to a solution ofmethyl 5-acetoxy-6-((trimethylsilyl)ethynyl)nicotinate (11.1 g, 38.09mmol, Step 3: Example 34) in MeOH at 0° C. and the reaction mixture wasstirred at RT for 2 h. The completion of the reaction was confirmed byTLC. The reaction mixture was concentrated, water was added, and theresulting mixture was extracted with DCM (2×300 mL). The combinedorganic layer was dried over Na₂SO₄ and concentrated. The crude residuewas purified by flash column chromatography using 30-35% EtOAc inpetroleum ether to afford the title compound. Yield: 52% (4.5 g, brownsolid). ¹H NMR (400 MHz, DMSO-d₆): δ 9.09 (d, J=2.0 Hz, 1H), 8.57 (d,J=2.4 Hz, 1H), 8.53 (d, J=1.2 Hz, 1H), 7.32-7.26 (m, 1H), 3.93 (s, 3H).LCMS: (Method A) 178.2 (M+H), Rt. 1.8 min, 88.2% (Max).

Step 5: methyl 2,3-dihydrofuro[3,2-b]pyridine-6-carboxylate

Methyl furo[3,2-b]pyridine-6-carboxylate (3.0 g, 16.93 mmol, Step 4:Example 34) was dissolved in MeOH (60 mL). Palladium on carbon (600 mg,10 wt %) was added and the reaction mixture was stirred under anatmosphere of hydrogen at 5 kg/cm² pressure, at 60° C. for 48 h. Aftercompletion (TLC), the catalyst was filtered off through a celite-pad,and the filtrate was concentrated to afford the title compound. Yield:60% (1.8 g, brown solid). ¹H NMR (400 MHz, DMSO-d₆): δ 8.54 (d, J=2.0Hz, 1H), 7.49 (d, J=1.2 Hz, 1H), 4.71 (t, J=12.0 Hz, 2H), 3.86 (s, 3H),3.34 (t, J=12.0 Hz, 2H). LCMS: (Method A) 180.2 (M+H), Rt. 1.7 min,97.7% (Max).

Step 6: (2,3-dihydrofuro[3,2-b]pyridin-6-yl)methanol

To a stirred solution of methyl2,3-dihydrofuro[3,2-b]pyridine-6-carboxylate (1.8 g, 10.04 mmol, Step 5:Example 34) in dry THF (18.0 mL) at −78° C. was added LAH (6.5 mL, 13.06mmol, 2.0 M in THF). The reaction mixture was stirred at RT for 2 h.After completion, the reaction mixture was quenched by addition of sat.aq. NH₄Cl, and the mixture was extracted by EtOAc (2×50 mL). Thecombined organic layer was washed with water (30 mL), brine (30 mL),dried over anhydrous Na₂SO₄ and concentrated under vacuum. The crudeproduct was purified by flash column chromatography using 60-70% ethylacetate in petroleum ether as eluent to afford the title compound.Yield: 80% (1.3 g, pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆): δ 7.92(s, 1H), 7.04 (s, 1H), 5.27-5.23 (m, 1H), 4.62 (t, J=9.2 Hz, 2H), 4.45(d, J=5.6 Hz, 2H), 3.22 (t, J=8.8 Hz, 2H). LCMS: (Method A) 152.2 (M+H),Rt. 0.5 min, 88.0% (Max).

Step 7: 2,3-dihydrofuro[3,2-b]pyridine-6-carbaldehyde

To a stirred solution of (2,3-dihydrofuro[3,2-b]pyridin-6-yl)methanol(1.3 g, 8.60 mmol, Step 6: Example 34) in DCM (26 mL, 20 V) at 0° C. wasadded Dess-Martin periodinane (4.74 g, 11.18 mmol) and the stirring wascontinued at RT for 2 h. After completion (TLC), the reaction mixturewas filtered, and the filtrate was washed with sat. aq. sodiumbicarbonate (50 mL), brine (30 mL), dried over anhydrous Na₂SO₄ andconcentrated under vacuum to afford the title compound. Yield: 79% (1.1g, pale yellow solid). ¹H NMR (400 MHz, DMSO-d₆): δ 10.02 (s, 1H), 8.55(d, J=2.0 Hz, 1H), 7.42 (d, J=2.0 Hz, 1H), 4.72 (t, J=12.0 Hz, 2H),3.41-3.30 (m, 2H).

Step 8: 1-(2,3-dihydrofuro[3,2-b]pyridin-6-yl)ethan-1-ol

To a stirred solution of 2,3-dihydrofuro[3,2-b]pyridine-6-carbaldehyde(1.0 g, 6.75 mmol, Step 7: Example 34) in dry THF (10 mL) at −20° C. wasadded MeMgBr (3.35 mL, 10.05 mmol, 3.0 M in THF). The reaction mixturewas stirred at RT for 2 h. After completion (TLC), the reaction mixturewas quenched by addition of saturated, aqueous NH4Cl solution, then thereaction mixture was extracted with EtOAc (2×60 mL). The combinedorganic layer was washed with water (50 mL), brine (30 mL), dried overanhydrous Na₂SO₄ and concentrated under vacuum. The crude material waspurified by flash column chromatography using 80-90% ethyl acetate inpet-ether as eluent affording the title compound. Yield: 63% (700 mg,pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆): δ 7.94 (d, J=2.0 Hz, 1H),7.06 (d, J=2.0 Hz, 1H), 5.23 (d, J=6.0 Hz, 1H), 4.71 (q, J=6.0 Hz, 1H),4.61 (t, J=11.6 Hz, 2H), 3.20 (t, J=11.6 Hz, 2H), 1.31 (d, J=8.4 Hz,3H). LCMS: (Method A) 166.3 (M+H), Rt. 0.55 min, 95.4% (Max).

Step 9: 6-(1-chloroethyl)-2,3-dihydrofuro[3,2-b]pyridine

To a stirred solution of1-(2,3-dihydrofuro[3,2-b]pyridin-6-yl)ethan-1-ol (100 mg, 0.60 mmol,Step 8: Example 34) in DCM (2.0 mL) at 0° C., was added thionyl chloride(0.15 mL, 1.81 mmol) drop wise and the reaction mixture was stirred for2 h at RT. Completion of the reaction was monitored by TLC. Aftercompletion, the reaction mixture was concentrated under vacuum,co-distilled with dry DCM (3×10 mL) and dried under vacuum to afford thetitle compound. Yield: 100% (120 mg, pale yellow gum). ¹H NMR (400 MHz,DMSO-d₆): δ 8.18 (s, 1H), 7.49 (s, 1H), 5.41 (q, J=6.4 Hz, 1H), 4.72 (t,J=8.8 Hz, 1H), 3.35 (dd, J=15.0, 4.0 Hz, 2H), 1.80 (d, J=6.8 Hz, 3H).LCMS: (Method A) 184.2 (M+H), Rt. 1.8 min, 89.1% (Max).

Example 1:5-(1-(7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[c][1,2,5]thiadiazole

To a stirred solution of Intermediate 1 (0.5 g, 2.52 mmol) in dry DMF(3.0 mL) under nitrogen atmosphere, were added triethylamine (1.0 mL7.19 mmol) and Intermediate 6 (0.44 g, 2.48 mmol) sequentially at RT.The reaction mixture was stirred overnight at 70° C. The completion ofthe reaction was monitored by TLC and the reaction mixture wasconcentrated under reduced pressure. The residue was diluted with waterand extracted with EtOAc. The combined organic layer was dried overanhydrous Na₂SO₄, filtered and concentrated. The resulting crude waspurified by Prep-HPLC (Method B) to give the title compound. Yield: 26%(220 mg, Pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆): δ 8.04 (d, J=9.2Hz, 1H), 7.94 (s, 1H), 7.88 (dd, J=1.6, 9.2 Hz, 1H), 6.97 (d, J=8.4 Hz,1H), 6.67 (d, J=2.8 Hz, 1H), 6.61 (dd, J=2.4, 8.2 Hz, 1H), 4.11-4.09 (m,1H), 3.68 (s, 3H), 2.81-2.76 (m, 4H), 2.63-2.51 (m, 4H), 1.41 (d, J=6.80Hz, 3H). LCMS: (Method A) 340.1 (M+H), Rt. 2.2 min, 98.7% (Max). HPLC:(Method A) Rt. 3.16 min, 98.1% (Max).

Example 2 and 3:(S)-5-(1-(7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[c][1,2,5]thiadiazoleand(R)-5-(1-(7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[c][1.2.5]thiadiazole

The enantiomers of Example 1 were separated by Chiral preparative SFC(Method A). The first peak was concentrated to give Example 2 and thesecond peak was concentrated to give Example 3.

Example 2: Yield: 38% (72 mg, pale brown gummy solid). ¹H NMR (400 MHz,DMSO-d₆): δ 8.03 (d, J=9.2 Hz, 1H), 7.94 (s, 1H), 7.88 (d, J=9.2 Hz,1H), 6.97 (d, J=8.0 Hz, 1H), 6.67 (d, J=2.4 Hz, 1H), 6.61 (dd, J=2.4,8.2 Hz, 1H), 4.10 (d, J=6.8 Hz, 1H), 3.68 (s, 3H), 2.81-2.76 (m, 4H),2.63-2.55 (m, 4H), 1.41 (d, J=6.80 Hz, 3H). LCMS: (Method A) 340.2(M+H), Rt. 2.2 min, 99.1% (Max). HPLC: (Method A) Rt. 3.1 min, 97.8%(Max). CHIRAL SFC: (Method A), Rt. 3.0 min, 99.1%. [α]²⁴D −11.00±0.00, c0.10 (MeOH).

Example 3: Yield: 34% (65 mg, pale brown gummy solid). ¹H NMR (400 MHz,DMSO-d₆): δ 8.03 (d, J=9.2 Hz, 1H), 7.93 (s, 1H), 7.87 (dd, J=1.2, 9.2Hz, 1H), 6.96 (d, J=8.0 Hz, 1H), 6.66 (d, J=2.8 Hz, 1H), 6.60 (q, J=2.4Hz, 1H), 4.09 (q, J=6.4 Hz, 1H), 3.67 (s, 3H), 2.81-2.75 (m, 4H),2.67-2.52 (m, 4H), 1.40 (d, J=6.80 Hz, 3H). LCMS: (Method A) 340.2(M+H), Rt. 2.2 min, 98.8% (Max). HPLC: (Method A), Rt. 3.1 min, 98.3%(Max). CHIRAL SFC: (Method A), Rt. 3.4 min, 99.1%.

Example 4:5-(1-(7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of Intermediate 2 (0.2 g, 1.01 mmol) in ACN (8mL), Intermediate 6 (0.215 g, 1.21 mmol) was added, followed by TEA(0.42 mL, 3.04 mmol) and the mixture was heated under reflux at 70° C.for 16 h. After completion (monitored by TLC), the reaction mixture wasconcentrated under vacuum. Water (20 mL) was added and was extractedwith EtOAc (2×25 mL). Combined organic layer was dried over anhydrousNa₂SO₄ and concentrated. The resulting crude product was purified byPrep-HPLC (Method B) to get the title compound. Yield: 40% (140 mg,brown gum). ¹H NMR (400 MHz, DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.0Hz, 1H), 8.02 (s, 1H), 7.53 (d, J=8.4 Hz, 1H), 6.96 (q, J=8.4 Hz, 1H),6.66 (d, J=2.4 Hz, 1H), 6.59 (dd, J=2.8, 8.0 Hz, 1H), 4.05 (q, J=6.8 Hz,1H), 3.67 (s, 3H), 2.80-2.78 (m, 4H), 2.60-2.58 (m, 4H), 1.42 (d, J=6.80Hz, 3H). LCMS: (Method A) 351.1 (M+H), Rt. 2.2 min, 99.7% (Max). HPLC:(Method A) Rt. 3.0 min, 99.8% (Max).

Example 5 and 6:(S)-5-(1-(7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazoleand(R)-5-(1-(7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

The enantiomers of Example 4 were separated by chiral preparative SFC(Method B). The first peak was concentrated and lyophilized to giveExample 5 and the second peak was concentrated and lyophilized to giveExample 6.

Example 5: Yield: 29% (36 mg, brown gum). ¹H NMR (400 MHz, DMSO-d₆): δ9.37 (s, 1H), 6.96 (d, J=8.0 Hz, 1H), 8.02 (s, 1H), 7.53 (d, J=8.4 Hz,1H), 6.96 (d, J=8.0 Hz, 1H), 6.66 (s, 1H), 6.59 (d, J=8.4 Hz, 1H), 4.05(q, J=6.8 Hz, 1H), 3.67 (s, 3H), 2.78 (t, J=5.6 Hz, 4H), 2.58 (t, J=8.0Hz, 4H), 1.42 (d, J=6.4 Hz, 3H). LCMS: (Method A) 339.1 (M+H), Rt. 2.1min, 99.9% (Max). HPLC: (Method A) Rt. 3.0 min, 99.5% (Max). Chiral SFC:(Method B) Rt. 4.6 min, 100% (Max). [α]²⁶D −0.35±0.00, c 0.56 (MeOH).

Example 6: Yield: 32% (39 mg, brown gum). ¹H NMR (400 MHz, DMSO-d₆): δ9.37 (s, 1H), 6.96 (d, J=8.4 Hz, 1H), 8.02 (s, 1H), 7.53 (d, J=8.4 Hz,1H), 6.96 (d, J=8.0 Hz, 1H), 6.66 (s, 1H), 6.59 (dd, J=2.4, 8.2 Hz, 1H),4.05 (q, J=7.2 Hz, 1H), 3.67 (s, 3H), 2.80-2.79 (m, 4H), 2.60-2.58 (m,4H), 1.42 (d, J=6.8 Hz, 3H). LCMS: (Method A) 339.1 (M+H), Rt. 2.1 min,99.8% (Max). HPLC: (Method A) Rt. 3.0 min, 98.0% (Max). Chiral SFC:(Method B) Rt. 5.6 min, 98.1% (Max).

Example 7:3-(1-(2,3-dihydrobenzofuran-6-yl)ethyl)-7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine

To a stirred solution of Intermediate 3 (0.4 g, 2.18 mmol) in ACN (10mL), Intermediate 6 (0.323 g, 1.82 mmol) was added, followed by TEA(0.92 mL, 6.57 mmol) and the reaction mixture was heated to reflux at70° C. 16 h. After completion (monitored by TLC), the reaction mixturewas evaporated under vacuum and water (20 mL) was added. The resultingmixture was extracted with EtOAc (2×25 mL), dried over anhydrous Na₂SO₄and concentrated. The resulting crude product was purified by Prep-HPLC(Method B) to get the title compound. Yield: 28% (198 mg, brown gum). ¹HNMR (400 MHz, DMSO-d₆): δ 7.12 (d, J=7.6 Hz, 1H), 6.96 (d, J=8.0 Hz,1H), 6.79-6.72 (m, 2H), 6.68-6.57 (m, 2H), 4.49 (t, J=8.4 Hz, 2H), 3.76(q, J=6.8 Hz, 1H), 3.68 (s, 3H), 3.12 (t, J=8.4 Hz, 2H), 2.79-2.68 (m,4H), 2.57-2.38 (m, 4H), 1.28 (d, J=6.8 Hz, 3H). LCMS: (Method A) 324.2(M+H), Rt. 2.3 min, 96.2% (Max). HPLC: (Method A) Rt. 3.4 min, 97.4%(Max).

Example 8 and Example 9:(S)-3-(1-(2,3-dihydrobenzofuran-6-yl)ethyl)-7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepineand(R)-3-(1-(2,3-dihydrobenzofuran-6-yl)ethyl)-7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine

The enantiomers of Example 7 were purified by chiral preparative SFC(Method C). The first peak was concentrated and lyophilised to giveExample 8 and the second peak was concentrated and lyophilised to giveExample 9.

Example 8: Yield: 40% (50 mg, Pale brown gum). ¹H NMR (400 MHz,DMSO-d₆): δ 7.12 (d, J=7.6 Hz, 1H), 6.96 (d, J=8.0 Hz, 1H), 6.79-6.72(m, 2H), 6.68-6.57 (m, 2H), 4.49 (t, J=8.4 Hz, 2H), 3.76 (q, J=6.8 Hz,1H), 3.68 (s, 3H), 3.12 (t, J=8.4 Hz, 2H), 2.79-2.68 (m, 4H), 2.57-2.38(m, 4H), 1.28 (d, J=6.8 Hz, 3H). LCMS: (Method A) 324.2 (M+H), Rt. 2.3min, 99.3% (Max). HPLC: (Method A) Rt. 3.3 min, 97.7% (Max). Chiral SFC(Method C) Rt. 3.0 min, 100.0% (Max). [α]²⁶D −6.92±0.54, c 0.13 (MeOH).

Example 9: Yield: 20% (19 mg, Pale brown gum). ¹H NMR (400 MHz,DMSO-d₆): δ 7.12 (d, J=7.6 Hz, 1H), 6.96 (d, J=8.0 Hz, 1H), 6.79-6.72(m, 2H), 6.68-6.57 (m, 2H), 4.49 (t, J=8.4 Hz, 2H), 3.76 (q, J=6.8 Hz,1H), 3.68 (s, 3H), 3.12 (t, J=8.4 Hz, 2H), 2.79-2.68 (m, 4H), 2.57-2.38(m, 4H), 1.28 (d, J=6.8 Hz, 3H). LCMS: (Method A) 324.2 (M+H), Rt. 2.3min, 99.3% (Max). HPLC: (Method A) Rt. 3.3 min, 98.2% (Max). Chiral SFC(Method C) Rt. 4.1 min, 96.9% (Max).

Example 10 and Example 11:5-(1-(6-chloro-7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazoleand5-(1-(7-chloro-8-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Step 1: 7-chloro-8-methoxy-2,3,4,5-tetrahydro-H-benzo[d]azepinehydrochloride 6-chloro-7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepinehydrochloride

To a stirred suspension of Intermediate 6 (0.2 g, 1.19 mmol) in glacialacetic acid (2 mL) was added SO₂Cl₂ (0.1 mL, 1.23 mmol) dropwise at RT.After stirring for 2.5 hours at RT. the reaction mixture wasconcentrated. The residue was co-distilled with toluene, dried undervacuum and was re-suspended in THF. Di-tert-butyl dicarbonate (0.37 mL,1.69 mmol) and triethylamine (0.32 mL, 2.30 mmol) were added and themixture was stirred at RT for 3 h and then concentrated. The residue wasdissolved in EtOAc and washed with sat. aq. Na₂CO₃ solution. Thecombined organic layer was dried over anhydrous Na₂SO₄, filtered andconcentrated. The resulting crude material was purified by flashchromatography (Silica gel: 230-400 mesh, Eluent: 15% ethyl acetate inpetroleum ether) to give the titled compounds as a mixture ofregioisomers. To a stirred solution of this mixture of regioisomers (230mg, 0.74 mmol) in dry 1,4 dioxane (1.0 mL) at 0□ was added HCl indioxane (4 M, 17 mL) and the reaction mixture was stirred at RT for 2 h.After completion of the reaction (monitored by TLC), the reactionmixture was concentrated under reduced pressure and it was trituratedwith ethyl acetate to get the title compounds as a mixture ofregioisomers (about 1:1 mixture calculated by ¹H NMR). Yield: 82% (230mg, pale brown solid). Regioisomer 1: ¹H NMR (400 MHz, DMSO-d₆): δ9.21-9.12 (m, 2H), 7.28 (s, 1H), 7.04 (s, 1H), 3.82 (s, 3H), 3.13-3.03(m, 8H). Regioisomer 2: ¹H NMR (400 MHz, DMSO-d₆): δ 9.21-9.12 (m, 2H),7.16 (d, J=11.2 Hz, 1H), 6.96 (d, J=11.2 Hz, 1H), 3.82 (s, 3H),3.13-3.03 (m, 8H). LCMS: (Method A) 212.1 (M+H), 1^(st) Rt. 1.4 min,42.0% (Max) and 2^(nd) Rt. 1.5 min, 47.7% (Max).

Step 2:5-(1-(6-chloro-7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazoleand5-(1-(7-chloro-8-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of Step 1: Example 10 (0.23 g, 1.08 mmol) in dryACN (3.0 mL) under nitrogen atmosphere, triethyl amine (TEA) (0.3 mL2.17 mmol), and Intermediate 2 (0.236 g, 1.19 mmol) were addedsequentially at RT. The reaction mixture was stirred overnight at 70° C.The completion of the reaction was monitored by TLC. The reactionmixture was evaporated under reduced pressure, water was added, and themixture was extracted with ethyl acetate. The combined organic layer wasdried over anhydrous Na₂SO₄, filtered and concentrated. The resultingcrude residue was purified by flash chromatography (Silica gel: 230-400mesh, Eluent: 45% ethyl acetate in petroleum ether) to give the titlecompound as a mixture of two regioisomers (Example 10:Example 11 ratioof 45:50). The regioisomers were separated by Prep-HPLC (Method A), andthe first peak was concentrated to give title compound Example 10. Thesecond peak was concentrated to give the title compound Example 11.

Example 10: Yield: 10% (22.0 mg, off white solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.01 (s, 1H), 7.51(dd, J=1.2, 8.4 Hz, 1H), 7.01 (d, J=8.0 Hz, 1H), 6.82 (d, J=8.4 Hz, 1H),4.03 (q, J=6.8 Hz, 1H), 3.77 (s, 3H), 3.09-2.83 (m, 4H), 2.68-2.51 (m,4H), 1.42 (d, J=6.8 Hz, 3H); LCMS: (Method A) 373.0 (M+H), Rt. 2.2 min,99.6% (Max). HPLC: (Method A) Rt. 3.2 min, 99.3% (Max).

Example 11: Yield: 20% (45 mg, off white solid); ¹H NMR (400 MHz,DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.03 (s, 1H), 7.53(dd, J=1.2, 8.4 Hz, 1H), 7.12 (s, 1H), 6.89 (s, 1H), 4.06 (q, J=6.8 Hz,1H), 3.78 (s, 3H), 2.85-2.76 (m, 4H), 2.61-2.51 (m, 4H), 1.42 (d, J=6.8Hz, 3H). LCMS: (Method A) 373.0 (M+H), Rt. 2.3 min, 98.2% (Max). HPLC:(Method A) Rt. 3.3 min 97.9% (Max).

Example 12:7-methoxy-3-(1-(quinoxalin-6-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

To a stirred solution of Intermediate 6 (0.14 g, 0.78 mmol), and TEA(0.54 mL, 3.39 mmol) in DMF (1.4 mL), was added Intermediate 4 (0.226 g,1.79 mmol) at RT and the mixture was stirred at 80° C. overnight. Aftercompletion (by TLC), the reaction mixture was concentrated at 50° C.under reduced pressure. The crude residue was suspended in water (10mL), extracted with EtOAc (2×50 mL), and the combined organic layer wasdried over Na₂SO₄ and concentrated. The crude material was purified byflash chromatography using 50-60% EtOAc in petroleum ether followed byfurther purification by Pep-HPLC (Method A) to get the tittle compound.Yield: 21% (56 mg, pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆): δ 8.92(d, J=6.8 Hz, 2H), 8.06 (d, J=8.4 Hz, 1H), 7.98 (d, J=8.8 Hz, 2H), 6.97(d, J=8.0 Hz, 1H), 6.66 (s, 1H), 6.60 (d, J=8.0 Hz, 1H), 4.16 (d, J=6.8Hz, 1H), 3.67 (s, 1H), 2.90-2.69 (m, 4H), 2.57-2.42 (m, 4H), 1.45 (d,J=6.4 Hz, 3H). LCMS: (Method A) 334.1 (M+H), Rt. 2.0 min, 97.6% (Max).HPLC: (Method A) Rt. 2.6 min, 98.0% (Max).

Example 13 and Example 14:5-(1-(7-bromo-1,3,4,5-tetrahydro-2H-benzo[c]azepin-2-yl)ethyl)benzo[d]thiazoleand5-(1-(7-bromo-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Step 1: 7-bromo-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride and7-bromo-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride

To a stirred solution of Intermediate 5 (0.4 g, 1.22 mmol) in 1,4dioxane (4 mL) was added HCl in dioxane (4 M, 4 mL) at 0° C. Thereaction mixture was stirred for 4 h at RT, while being monitored byTLC. After completion, the reaction mixture was concentrated underreduced pressure to get the tittle compound. Yield: 95% (0.3 g, offwhite solid). LCMS: (Method A) 227.9 (M+H), Rt. 1.9 min, 83.2% (Max)(single peak observed under these LC conditions).

Step 2:5-(1-(7-bromo-1,3,4,5-tetrahydro-2H-benzo[c]azepin-2-yl)ethyl)benzo[d]thiazoleand5-(1-(7-bromo-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of Step 1: Example 13 (0.27 g, 1.0 mmol), TEA (0.4mL, 2.6 mmol) in DMF (3 mL), Intermediate 2 (0.25 g, 1.3 mmol) was addedat RT and the mixture was stirred at 70° C. for overnight. Completion ofthe reaction was monitored by TLC and the reaction mixture wasconcentrated at 50° C. under reduced pressure. The residue was suspendedwith water (10 mL), extracted with EtOAc (2×25 mL), and the combinedorganic layer was dried over Na₂SO₄ and concentrated. The resultingcrude material was purified by flash chromatography using 1-2% MeOH inDCM to get the mixture of regioisomers. Yield: 22% (87 mg, pale browngummy solid). The regioisomers were separated by Prep-HPLC (Method B)and the first fraction was collected to get Example 13, and the secondfraction was collected to get tittle compound Example 14.

Example 13: Yield: 4% (13 mg, pale brown solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.38 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 7.95 (s, 1H), 7.45 (d,J=8.4 Hz, 1H), 7.41 (s, 1H), 7.27-7.24 (m, 1H), 6.80 (d, J=8.0 Hz, 1H),3.92 (d, J=14.8 Hz, 1H), 3.77-3.75 (m, 1H), 3.65 (d, J=14.4 Hz, 1H),3.18-3.07 (m, 1H), 2.99-2.94 (m, 1H), 2.88-2.85 (m, 2H), 1.67-1.66 (m,1H), 1.62-1.58 (m, 1H), 1.3 (d, J=6.8 Hz, 3H). LCMS: (Method A) 388.9(M+H), Rt. 2.3 min, 99.6% (Max). HPLC: (Method A) Rt. 3.4 min, 99.9%(Max).

Example 14: Yield: 4% (16 mg, pale brown solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.0 Hz, 1H), 8.03 (s, 1H), 7.53 (d,J=8.4 Hz, 1H), 7.29 (s, 1H), 7.25-7.22 (m, 1H), 7.03 (d, J=8.4 Hz, 1H),4.09-4.04 (m, 1H), 2.83-2.83 (m, 4H), 2.60-2.50 (m, 4H), 1.41 (d, J=6.8Hz, 3H). LCMS: (Method A) 388.9 (M+H), Rt. 2.3 min, 98.9% (Max). HPLC:(Method A) Rt. 3.5 min, 98.5% (Max).

Example 15 and Example 16:2-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepine-7-carbonitrileand3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine-7-carbonitrile

Step 1: tert-butyl7-cyano-1,3,4,5-tetrahydro-2H-benzo[c]azepine-2-carboxylate andtert-butyl 7-cyano-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate

To a stirred solution of Intermediate 5 (1.0 g, 3.07 mmol) in DMF (3mL), was added Zn(CN)₂ (0.72 g, 6.15 mmol) at RT and the solution waspurged with nitrogen for 10 min. Then PdCl₂(dppf).DCM-complex (0.25 g,0.31 mmol) was added and the reaction mixture was stirred at 120° C. forovernight. After completion, (by TLC) and the reaction mixture wassuspended with water (10 mL), and extracted with EtOAc (2×50 mL). Thecombined organic layer was dried over Na₂SO₄ and concentrated. Theresulting crude material was purified by flash chromatography using50-60% EtOAc in Pet-Ether to afford the tittle compound as a mixture ofregioisomers. Yield: 61% (0.51 g, pale brown gummy solid). LCMS: (MethodA) 173.1 (M-Boc), Rt. 3.0 min, 93.1% (Max).

Step 2: 2,3,4,5-tetrahydro-1H-benzo[d]azepine-7-carbonitrilehydrochloride and 2,3,4,5-tetrahydro-1H-benzo[c]azepine-6-carbonitrilehydrochloride

To a stirred solution of Step 1: Example 15 (0.5 g, 1.83 mmol) in 1,4dioxane (5 mL) was added HCl in dioxane (4 M, 5 mL) at 0□. The reactionmixture was stirred for 4 h at RT while being monitored by TLC. Aftercompletion, the reaction mixture was concentrated under reduced pressureto get the tittle compound as a mixture of regioisomers. Yield: 78% (0.3g, off white solid). LCMS: (Method A) 173.1 (M+H), Rt. 1.5 min, 92.1%(Max).

Step 3:2-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepine-7-carbonitrileand3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine-7-carbonitrile

To a stirred solution of Step 2: Example 15 (0.3 g, 1.73 mmol), TEA (0.5mL, 3.6 mmol) in DMF (3 mL), Intermediate 2 (0.34 g, 1.72 mmol) wasadded at RT and the reaction mixture was stirred at 70° C. forovernight. The reaction was monitored by TLC, upon completion, thereaction mixture was evaporated at 50° C. under reduced pressure. Theresidue was suspended with water (10 mL), extracted with EtOAc (2×25mL), and the combined organic layer was dried over Na₂SO₄ andconcentrated. The resulting crude residue was purified by flashchromatography using 1-2% MeOH in DCM to get the title compound as amixture of regioisomers. Yield: 25% (120 mg, pale brown gummy solid).The regioisomers were separated by SFC (Method E). The first fractionwas collected to get Example 15 and the second fraction was collected toget Example 16.

Example 15: Yield: 13% (14 mg, Off white solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.37 (s, 1H), 8.10-8.07 (m, 1H), 7.94 (s, 1H), 7.65 (s, 1H),7.54 (d, J=7.6 Hz, 1H), 7.43 (d, J=8.4 Hz, 1H), 7.05 (d, J=6.0 Hz, 1H),4.00 (d, J=14.4 Hz, 1H), 3.78-3.70 (m, 2H), 3.15-3.05 (m, 1H), 2.98-2.92(m, 3H), 1.67-1.62 (m, 2H), 1.36-1.34 (m, 3H). LCMS: (Method A) 334.1(M+H), Rt. 1.77 min, 98.8% (Max). HPLC: (Method A) Rt. 2.71 min, 97.6%(Max).

Example 16: Yield: 13% (21 mg, Off white solid). ¹H NMR (400 MHz,DMSO-d₆): 9.36 (s, 1H), 8.08 (d, J=8.4 Hz, 1H), 8.02 (s, 1H), 7.54-7.51(m, 3H), 7.28 (d, J=7.6 Hz, 1H), 4.08-4.07 (m, 1H), 2.92-2.85 (m, 4H),2.67-2.66 (m, 2H), 2.54-2.52 (m, 2H), 1.41 (d, J=6.8 Hz, 3H). LCMS:(Method A) 334.2 (M+H), Rt. 1.9 min, 98.3% (Max). HPLC: (Method A) Rt.2.7 min, 98.2% (Max).

Example 17 and Example 18:5-(1-(7-(methylsulfonyl)-1,3,4,5-tetrahydro-2H-benzo[c]azepin-2-yl)ethyl)benzo[d]thiazoleand5-(1-(7-(methylsulfonyl)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Step 1: tert-butyl7-(methylthio)-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate andtert-butyl7-(methylthio)-1,3,4,5-tetrahydro-2H-benzo[c]azepine-2-carboxylate

To a stirred solution of Intermediate 5 (0.6 g, 1.84 mmol) in THF (6mL), n-BuLi (1.22 mL, 3.05 mmol) was added at −78° C. and the reactionmixture was stirred at −78° C. for 30 min. Then Me₂S₂ was added slowlyat −78° C. and the mixture was stirred for another 30 min. Aftercompletion (TLC), the reaction mixture was quenched with aq. NH₄Clsolution (10 mL), extracted with EtOAc (2×50 mL), and the combinedorganic layer was dried over sodium sulphate and concentrated. Theresulting crude material was purified by flash chromatography using50-60% EtOAc in pet-ether to afford the tittle compound as a mixture ofregioisomers. Yield: 75% (0.41 g, pale brown gummy solid). LCMS: (MethodA) 194.1 (M+H), Rt. 3.2 min, 96.7% (Max).

Step 2: tert-butyl7-(methylsulfonyl)-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylateand tert-butyl7-(methylsulfonyl)-1,3,4,5-tetrahydro-2H-benzo[c]azepine-2-carboxylate

To a stirred solution of Step 1: Example 17 (0.4 g, 2.06 mmol) in DCM (4mL), mCPBA (0.73 g, 4.22 mmol) was added at 0° C. and the reactionmixture was stirred at RT for 1 h. Completion of the reaction wasmonitored by TLC. The reaction mixture was quenched with sat. aq. NaHCO₃solution (10 mL), extracted with DCM (2×25 mL), and the combined organiclayer was dried over Na₂SO₄ and concentrated to afford the tittlecompound as a mixture of regioisomers. Yield: 45% (0.42 g, colorlessliquid). LCMS: (Method A) 226.0 (M-Boc), Rt. 2.7 min, 96.0% (Max).

Step 3: 7-(methylsulfonyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepinehydrochloride and7-(methylsulfonyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride

To a stirred solution of Step 2: Example 17 (0.4 g, 1.23 mmol) in1,4-dioxane (4 mL) was added HCl in dioxane (4 M, 4 mL) at 0□. Thereaction mixture was stirred for 4 h at RT while being monitored by TLC.After completion, the reaction mixture was concentrated under reducedpressure to get the tittle compounds as a mixture of regioisomers.Yield: 91% (0.3 g, off white solid). LCMS: (Method A) 226.0 (M+H), Rt.1.0 min, 88.5% (Max).

Step 4:5-(1-(7-(methylsulfonyl)-1,3,4,5-tetrahydro-2H-benzo[c]azepin-2-yl)ethyl)benzo[d]thiazoleand5-(1-(7-(methylsulfonyl)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of Step 3: Example 17 (0.3 g, 1.15 mmol), TEA (0.4mL, 2.87 mmol) in DMF (3 mL), 5-(1-chloroethyl)benzo[d]thiazole(Intermediate 2) (0.27 g, 1.37 mmol) was added at RT and the reactionmixture was stirred at 70° C. for overnight. After completion, thereaction mixture was evaporated at 50° C. under reduced pressure. Theresidue was suspended with water (10 mL), extracted with EtOAc (2×25mL), and the combined organic layer was dried over Na₂SO₄ andconcentrated. The resulting crude material was purified by flashchromatography using 1-2% MeOH in DCM to get the title compounds as amixture of regioisomers. Yield: 45% (200 mg, pale brown gummy solid).The regioisomers were separated by SFC (Method F). The first fractionwas collected to get Example 17 and the second fraction was collected toget Example 18.

Example 17: Yield: 14% (63 mg, Off white solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.38 (s, 1H), 8.10 (d, J=8.4 Hz, 1H), 7.97 (s, 1H), 7.73 (s,1H), 7.64-7.62 (m, 1H), 7.46 (d, J=8.4 Hz, 1H), 7.14 (d, J=7.6 Hz, 1H),4.02 (d, J=14.4 Hz, 1H), 3.84-3.73 (m, 2H), 3.21 (s, 3H), 3.09-2.97 (m,4H), 1.71-1.65 (m, 2H), 1.38 (d, J=6.4 Hz, 3H). LCMS: (Method B) 387.1(M+H), Rt. 2.9 min, 98.2% (Max). HPLC: (Method B) Rt. 5.6 min, 98.9%(Max).

Example 18: Yield: 10% (46 mg, Off white solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.36 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.03 (s, 1H), 7.63 (s,1H), 7.62-7.60 (m, 1H), 7.53 (d, J=8.4 Hz, 1H), 7.34 (d, J=8.0 Hz, 1H),4.09-4.08 (m, 1H), 3.14 (s, 3H), 2.96-2.93 (m, 4H), 2.66-2.49 (m, 4H),1.42 (d, J=6.80 Hz, 3H). LCMS: (Method B) 387.1 (M+H), Rt. 2.6 min,96.9% (Max). HPLC: (Method B) Rt. 5.6 min, 95.1% (Max).

Example 19:5-(1-(7-methoxy-2-methyl-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of Intermediate 8 (0.27 g, 1.37 mmol), TEA (0.5mL, 3.5 mmol) in DMF (3 mL), Intermediate 2 (0.33 g, 1.67 mmol) wasadded at RT and stirred at 70° C. for overnight. Completion of thereaction was monitored by TLC and the reaction mixture was concentratedat 50° C. under reduced pressure. The residue was suspended in water (10mL), extracted with EtOAc (2×50 mL), and the combined organic layer wasdried over Na₂SO₄ and concentrated. The resulting crude was purified byPep-HPLC (Method B) to get the tittle compound as mixture ofdiastereomers in 1:1.2 ratio. Yield: 8% (40 mg, pale brown gummy solid).¹H NMR (400 MHz, DMSO-d₆): δ 9.38 (s, 1H), 8.13-8.05 (m, 2H), 7.55 (d,J=8.0 Hz, 1H), 6.96-6.91 (m, 1H), 6.64-6.63 (m, 2H), 4.16-4.09 (m, 1H),3.70 (s, 3H), 3.29-1.17 (m, 2H), 2.98-2.84 (m, 2H), 2.68-2.65 (m, 1H),2.50-2.40 (m, 2H), 1.38-1.33 (m, 3H), 0.76-0.74 (m, 3H). LCMS: (MethodA) 353.1 (M+H), Rt. 3.0 min, 94.6% (Max). HPLC: (Method A) Rt. 3.2 min,99.6% (Max) (single peak observed under these LC conditions).

Example 20:5-(1-(1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of 2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.2 g,1.36 mmol), and TEA (0.5 mL, 3.4 mmol) in DMF (2 mL), were addedIntermediate 2 (0.32 g, 1.6 mmol) at RT and the mixture was stirred at70 □ for overnight. Completion of the reaction was monitored by TLC. Thereaction mixture was concentrated at 50° C. under reduced pressure. Theresidue was suspended in water (10 mL), extracted with EtOAc (2×25 mL),and the combined organic layer was dried over Na₂SO₄ and concentrated.The resulting crude was purified by flash chromatography using 1-2% MeOHin DCM to get the tittle compound. Yield: 48% (0.2 g, off white solid).¹H NMR (400 MHz, DMSO-d₆): δ 9.36 (s, 1H), 8.08 (d, J=8.4 Hz, 1H), 8.02(s, 1H), 7.53 (d, J=8.4 Hz, 1H), 7.04 (s, 4H), 4.06-4.05 (m, 1H),2.84-2.82 (m, 4H), 2.63-2.59 (m, 2H), 2.59-2.50 (m, 2H), 1.41 (d, J=6.8Hz, 3H). LCMS: (Method A) 309.2 (M+H), Rt. 2.2 min, 96.7% (Max). HPLC:(Method A) Rt. 2.9 min, 97.4% (Max).

Example 21 and Example 22:(S)-5-(1-(1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazoleand(R)-5-(1-(1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Enantiomers of Example 20 were separated by chiral preparative SFC(Method D). The first fraction was collected to get Example 21 and thesecond fraction was collected to get Example 22.

Example 21: Yield: 48% (0.05 g, pale brown gummy solid). ¹H NMR (400MHz, DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.03 (s, 1H),7.55-7.53 (m, 1H), 7.05 (s, 4H), 4.09-4.04 (m, 1H), 2.85-2.83 (m, 4H),2.64-2.63 (m, 2H), 2.59-2.50 (m, 2H), 1.42 (d, J=6.8 Hz, 3H). LCMS:(Method A) 309.2 (M+H), Rt. 1.6 min, 99.4% (Max). HPLC: (Method A) Rt.3.0 min, 99.3% (Max). Chiral SFC: (Method D) Rt. 4.2 min, 100% (Max).[α]²⁶D −3.77±0.17, c 0.52 (MeOH).

Example 22: Yield: 48% (0.05 g, pale brown gummy solid). ¹H NMR (400MHz, DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.03 (s, 1H),7.55-7.53 (m, 1H), 7.05 (s, 4H), 4.09-4.04 (m, 1H), 2.85-2.83 (m, 4H),2.60-2.58 (m, 2H), 2.58-2.50 (m, 2H), 1.42 (d, J=6.8 Hz, 3H). LCMS:(Method A) 309.2 (M+H), Rt. 1.6 min, 99.5% (Max). HPLC: (Method A) Rt.2.9 min, 98.8% (Max). Chiral SFC: (Method D) Rt. 4.6 min, 97.3% (Max).

Example 23:5-(1-(7-((6-fluoropyridin-2-yl)oxy)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol(100 mg, 0.30 mmol, Example 33) in dry THF (1 mL) at 0° C. was added NaH(22 mg, 0.46 mmol) and the reaction mixture was stirred for 1 h at RT.2,6-Difluoropyridine (35 mg, 0.30 mmol) was added into the reactionmixture and the stirring was continued for another 2 h. After completion(TLC), the reaction mixture was quenched by ice and extracted with EtOAc(2×50 mL). The combined organic layer was dried over Na₂SO₄ andconcentrated. The crude residue was purified by Biotage isolera using50-60% EtOAc in petroleum ether to afford the title compound. Yield: 10%(9 mg, pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆): δ 9.36 (s, 1H), 8.09(d, J=8.4 Hz, 1H), 8.03 (s, 1H), 7.98-7.96 (m, 1H), 7.54 (d, J=8.4 Hz,1H), 7.12 (d, J=8.0 Hz, 1H), 6.89 (d, J=2.4 Hz, 1H), 6.85-6.83 (m, 3H),4.07 (q, J=6.8 Hz, 1H), 2.91-2.81 (m, 4H), 2.67-2.55 (m, 4H), 1.42 (d,J=6.8 Hz, 3H). LCMS: (Method A) 420.0 (M+H), Rt. 2.5 min, 99.5% (Max).HPLC: (Method A) Rt. 3.6 min, 99.9% (Max), 99.8% (220 nm).

Example 24:5-(1-(7-(difluoromethoxy)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Step 1: 7-hydroxy-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one

To a stirred solution of8-methoxy-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one (1.0 g, 5.23 mmol,Step 3: Intermediate 6) in DCM (10 mL), was added BBr₃ (7.84 mL, 1.0 Msolution in DCM, 7.84 mmol) at 0□ and the mixture was stirred at RT forovernight. After completion (TLC), the reaction mixture was quenched bymethanol at 0□ and then concentrated under reduced pressure. Theresulting solid was triturated with hexane-diethyl ether (8:2) to givethe title compound. Yield: 77% (720 mg, brown gum). ¹H NMR (400 MHz,DMSO-d₆): δ 7.54 (s, 1H), 6.90 (d, J=8.0 Hz, 1H), 6.57 (d, J=8.0 Hz,1H), 6.49 (s, 1H), 3.60 (s, 2H), 3.38-3.37 (m, 2H), 2.88-2.86 (m, 2H).LCMS: (Method A) 178.2 (M+H), Rt. 1.5 min, 63.9% (Max).

Step 2: 7-(difluoromethoxy)-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one

To a stirred solution of7-hydroxy-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one (0.2 g, 1.04 mmol,Step 1: Example 24) in ACN (2.0 mL) and H₂O (0.4 mL) at 0° C., wereadded KOH (171 mg, 3.05 mmol) and diethyl(bromodifluoromethyl)phosphonate (419 mg, 1.57 mmol). The reactionmixture was stirred at RT for overnight while being monitored by TLC.After completion, the reaction mixture was diluted with water andextracted with EtOAc (2×50 mL). The combined organic layer was driedover Na₂SO₄ and concentrated. The crude residue was purified by Biotageisolera using 50-60% EtOAc in petroleum ether as eluent to get thetittle compound. Yield: 87% (180 mg, brown gum). LCMS: (Method A) 228.2(M+H), Rt. 2.2 min, 71.6% (Max).

Step 3: 7-(difluoromethoxy)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

To a stirred solution of7-(difluoromethoxy)-1,3,4,5-tetrahydro-2H-benzo[d]azepin-2-one (180 mg,0.79 mmol, Step 2: Example 24) in THF (6 mL) was added a solution ofBH₃-THF (1.0 M, 1.18 mL, 1.18 mmol) at 0□ and the reaction mixture wasstirred at 65□ for overnight. After completion (TLC), the reactionmixture was slowly quenched with methanol (6 mL) at 0□ followed by 1.5 NHCl (6 mL) at RT and then the mixture was heated to 50° C. for 1 h. Thereaction mixture was then concentrated under reduced pressure to affordthe crude tittle compound which was directly used in the next step.Yield: 77% (130 mg, pale brown gum).

Example 24:5-(1-(7-(difluoromethoxy)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of7-(difluoromethoxy)-2,3,4,5-tetrahydro-1H-benzo[d]azepine (130 mg, 0.61mmol, Step 3: Example 24) and TEA (0.25 mL, 1.83 mmol) in DMF (1.3 mL),was added 5-(1-chloroethyl)benzo[d]thiazole, Intermediate 2, (145 mg,0.73 mmol) at RT and the reaction mixture was stirred at 80 □ forovernight. After completion (TLC), the reaction mixture was concentratedunder reduced pressure. The residue was suspended with water (10 mL),extracted with EtOAc (2×50 mL). The combined organic layer was driedover Na₂SO₄ and concentrated. The crude residue was purified by Biotageisolera using 50-60% EtOAc in petroleum ether as the eluent to get thetittle compound. Yield: 13% (19 mg, pale yellow gum). ¹H NMR (400 MHz,DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.03 (s, 1H), 7.53(dd, J=8.4 Hz, 1.2 Hz, 1H), 7.30-6.93 (m, 2H), 6.92-6.82 (m, 2H), 4.07(q, J=6.8 Hz, 1H), 2.90-2.69 (m, 4H), 2.68-2.51 (m, 4H), 1.42 (d, J=6.8Hz, 3H). LCMS: (Method A) 375.1 (M+H), Rt. 1.7 min, 94.6% (Max). HPLC:(Method A) Rt. 3.4 min, 96.6% (Max), 96.6% (220 nm).

Example 25:5-(1-(7-isopropoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Step 1: tert-butyl7-isopropoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate

To a stirred solution of tert-butyl7-hydroxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate,Intermediate 7, (300 mg, 1.14 mmol) in DMF (3.0 mL), were added K₂CO₃(472 mg, 3.42 mmol) and 2-bromopropane (210 mg, 1.70 mmol) at RT and thereaction mixture was stirred at 80° C. for overnight. After completion(TLC), the reaction mixture was concentrated under reduced pressure at50° C. The residue was suspended with water (10 mL) and extracted withEtOAc (2×60 mL). The combined organic layer was dried over Na₂SO₄ andconcentrated to get tittle compound. Yield: 43% (300 mg, pale yellowgum). LCMS: (Method A) 206.4 (M-Boc+H), Rt. 3.3 min, 27% (Max).

Step 2: 7-isopropoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride

To a stirred solution of tert-butyl7-isopropoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate, Step1: Example 25, (300 mg, 0.98 mmol) in 1,4 dioxane (1.0 mL) was added HClin 1,4-dioxane (4 M, 1.0 mL) at 0° C. The reaction mixture was stirredfor 4 h at RT. After completion (TLC), the reaction mixture wasconcentrated under reduced pressure and was triturated with EtOAc to getthe tittle compound. Yield: 93% (110 mg, off white solid). LCMS: (MethodA) 206.4 (M+H), Rt. 1.9 min, 36% (Max).

Example 25:5-(1-(7-isopropoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of7-isopropoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride, Step2: Example 25, (180 mg, 0.87 mmol) in dry DMF (2 mL), were added5-(1-chloroethyl)benzo[d]thiazole (250 mg, 0.96 mmol) and TEA (0.25 mL,1.74 mmol) and the mixture was heated at 70° C. for overnight. Aftercompletion (TLC), the reaction mixture was concentrated under vacuum. Tothe resulting residue, water was added, and the aqueous layer wasextracted with EtOAc (2×20 mL). The combined organic layer was washedwith water (10 mL), dried over Na₂SO₄ and concentrated. The cruderesidue was purified by prep. HPLC (Method A) to afford the titlecompound. Yield: 11% (13 mg, pale yellow gum). ¹H NMR (400 MHz,DMSO-d₆): δ 9.36 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.01 (s, 1H), 7.52 (d,J=8.4 Hz, 1H), 6.92 (d, J=8.0 Hz, 1H), 6.65-6.60 (m, 1H), 6.56 (dd,J=8.0 Hz, 2.4 Hz, 1H), 4.49 (h, J=6.4 Hz, 1H), 4.09-4.00 (m, 1H),2.82-2.70 (m, 4H), 2.66-2.48 (m, 4H), 1.41 (d, J=6.8 Hz, 3H), 1.22-1.13(m, 6H). LCMS: (Method A) 367.2 (M+H), Rt. 2.3 min, 99.5% (Max). HPLC:(Method A) Rt. 3.7 min, 99.1% (Max), 99.0% (220 nm).

Example 26:5-(1-(7-isobutoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Step 1: tert-butyl7-isobutoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate

To a stirred solution of tert-butyl7-hydroxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate (300 mg,1.14 mmol, Intermediate 7) in DMF (3.0 mL), were added K₂CO₃ (472 mg,3.42 mmol) and 1-bromo-2-methylpropane (230 mg, 1.70 mmol) at RT and themixture was stirred at 80° C. for overnight. After (TLC) the reactionmixture was concentrated under reduced pressure. The residue wassuspended with water (10 mL), extracted with EtOAc (2×60 mL). Thecombined organic layer was dried over Na₂SO₄ and concentrated to get thetittle compound. Yield: 49% (360 mg, pale yellow gum). LCMS: (Method A)220.4 (M-Boc+H), Rt. 3.56 min, 35% (Max).

Step 2: 7-isobutoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride

To a stirred solution of tert-butyl7-isobutoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate (360 mg,0.98 mmol, Step 1—Example 26) in 1,4 dioxane (1.2 mL) was added HCl in1,4 dioxane (4 M, 1.2 mL) at 0° C. The reaction mixture was stirred forat RT 4 h. After completion (TLC), the reaction mixture was concentratedunder reduced pressure and the residue was triturated with EtOAc to getthe tittle compound. Yield: 93% (110 mg, off white solid). LCMS: (MethodA) 220.3 (M+H), Rt. 2.17 min, 47% (Max).

Example 26:5-(1-(7-isobutoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

To a stirred solution of7-isobutoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride (360 mg,1.42 mmol, Step 2: Example 26) in dry DMF (3.6 mL), were added5-(1-chloroethyl)benzo[d]thiazole (309 mg, 1.56 mmol) and TEA (0.59 mL,4.26 mmol) and the reaction mixture was heated at 70° C. for overnight.After completion (TLC), the reaction mixture was concentrated undervacuum. The crude residue was diluted with water and was extracted withEtOAc (2×20 mL). The combined organic layer was washed with water (10mL), dried over Na₂SO₄ and concentrated. The crude residue was purifiedby prep. HPLC (Method A) to afford title compound. Yield: 38% (75 mg,pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆): δ 9.37 (s, 1H), 8.09 (d,J=8.4 Hz, 1H), 8.02 (d, J=0.8 Hz, 1H), 7.53 (dd, J=8.4 Hz, 1.2 Hz, 1H),6.94 (d, J=8.4 Hz, 1H), 6.65 (d, J=2.4 Hz, 1H), 6.58 (dd, J=8.0 Hz, 2.8Hz, 1H), 4.06 (q, J=6.8 Hz, 1H), 3.65 (d, J=6.4 Hz, 2H), 2.87-2.72 (m,4H), 2.66-2.53 (m, 4H), 1.95 (h, J=6.8 Hz, 1H), 1.41 (d, J=6.8 Hz, 3H),0.94 (d, J=6.8 Hz, 6H). LCMS: (Method A) 381.1 (M+H), Rt. 3.5 min, 97.4%(Max).

HPLC: (Method A) Rt. 4.1 min, 96.5% (Max), 97.3% (220 nm).

Example 27:(R)-5-(1-(7-isobutoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazoleor(S)-5-(1-(7-isobutoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Enantiomers of Example 26 were separated by chiral preparative SFC(Method G). The second fraction was collected to get Example 27.

Example 27: Yield: 19% (16 mg, pale yellow gum). ¹H NMR (400 MHz,DMSO-d₆): δ 9.42 (s, 1H), 8.14 (d, J=8.4 Hz, 1H), 8.08 (s, 1H), 7.59(dd, J=8.4 Hz, 1.2 Hz, 1H), 6.99 (d, J=8.0 Hz, 1H), 6.70 (d, J=2.4 Hz,1H), 6.64 (dd, J=8.4 Hz, 2.4 Hz, 1H), 4.11 (q, J=6.8 Hz, 1H), 3.70 (d,J=6.4 Hz, 2H), 2.90-2.75 (m, 4H), 2.72-2.57 (m, 4H), 2.01 (h, J=6.4 Hz,1H), 1.47 (d, J=6.8 Hz, 3H), 0.99 (d, J=6.8 Hz, 6H). LCMS: (Method A)381.2 (M+H), Rt. 2.6 min, 99.1% (Max). HPLC: (Method A) Rt. 4.1 min,97.5% (Max), 98.4% (220 nm). Chiral SFC: (Method G) Rt. 4.1 min, 99.6%(Max).

Example 28:5-((7-methoxy-2-methyl-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)methyl)benzo[c][1,2,5]thiadiazole

Step 1: benzo[c][1,2,5]thiadiazol-5-ylmethanol

To a stirred solution of benzo[c][1,2,5]thiadiazole-5-carbaldehyde (1.0g, 6.09 mmol) in MeOH (8 mL) was added NaBH₄ (0.25 g, 6.71 mmol) at 0□and the reaction mixture was stirred for 1 h at RT. After completion(TLC), and the reaction mixture was diluted with water (20 mL) andextracted with EtOAc (2×50 mL). The combined organic layer was driedover Na₂SO₄ and concentrated to afford tittle compound. Yield: 71% (0.72g, off white solid). ¹H NMR (400 MHz, DMSO-d₆): δ 8.06-8.03 (m, 1H),7.96-7.87 (m, 1H), 7.68-7.65 (m, 1H), 5.55 (t, J=7.6 Hz, 1H), 4.71 (d,J=9.2 Hz, 2H). LCMS: (Method A) No ionisation (M+H), Rt. 1.3 min, 95.4%(Max).

Step 2: 5-(chloromethyl)benzo[c][1,2,5]thiadiazole

To a stirred solution of Step 1: Example 29(benzo[c][1,2,5]thiadiazol-5-ylmethanol) (0.40 g, 2.42 mmol) in dry DCM(4 mL), was added thionyl chloride (0.6 mL, 7.22 mmol) slowly at 0° C.The reaction mixture was stirred at RT for 1 h. The reaction mixture wasconcentrated under vacuum and the resulting residue was diluted with DCM(50 mL). The DCM layer was washed with water (2×10 mL), brine solution(20 mL), dried over anhydrous sodium sulphate and concentrated undervacuum to give tittle compound. Yield: 94% (0.42 g, off white solid). ¹HNMR (400 MHz, DMSO-d₆): δ 8.18-8.13 (m, 1H), 8.10-8.04 (m, 1H),7.78-7.75 (m, 1H), 4.99 (s, 2H). LCMS: (Method A) No ionisation (M+H),Rt. 2.1 min, 85.9% (Max).

Step 3:5-((7-methoxy-2-methyl-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)methyl)benzo[c][1,2,5]thiadiazole

To a stirred solution of Intermediate 8 (0.27 g, 1.41 mmol), TEA (0.6mL, 4.24 mmol) in ACN (3 mL), was added Step 2: Example 29,5-(chloromethyl)benzo[c][1,2,5]thiadiazole, (0.28 g, 1.55 mmol) at roomtemperature and stirred at RT for 48 h. The reaction was monitored byTLC, after completion, the reaction mixture was concentrated at 50° C.under reduced pressure. The residue was suspended with water (10 mL),and extracted with EtOAc (2×25 mL). The combined organic layer was driedover Na₂SO₄ and concentrated. The resulting crude material was purifiedby flash chromatography using 1-2% MeOH in DCM to get the tittlecompound. Yield: 30% (0.14 g, pale brown gum). ¹H NMR (400 MHz,DMSO-d₆): δ 8.06 (d, J=8.0 Hz, 1H), 8.00 (s, 1H), 7.79 (d, J=8.8 Hz,1H), 6.98 (d, J=8.0 Hz, 1H), 6.68-6.64 (m, 2H), 4.00-3.87 (m, 2H), 3.61(s, 3H), 3.28-3.24 (m, 1H), 3.16-3.13 (m, 1H), 3.02-2.99 (m, 1H),2.72-2.62 (m, 2H), 2.60-2.51 (m, 2H), 0.79 (d, J=6.80 Hz, 3H). LCMS:(Method A) 340.2 (M+H), Rt. 1.6 min, 97.1% (Max). HPLC: (Method A) Rt.3.1 min, 97.1% (Max).

Example 29:5-((7-methoxy-2-methyl-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)methyl)benzo[d]thiazole

Step 1: benzo[d]thiazol-5-ylmethanol

To a stirred solution of methyl benzo[d]thiazole-5-carboxylate (1.0 g,5.18 mmol) in THF (10 mL) was added a solution of LAH in THF (1.0 M,6.22 mL, 6.22 mmol) at −78□ and the reaction mixture was stirred for 1 hat −78□. Upon completion (TLC), the reaction mixture was quenched withsat. aq. NH₄Cl (10 mL) and extracted with EtOAc (2×25 mL). The combinedorganic layer was dried over Na₂SO₄ and concentrated. The resultingcrude material was purified by Biotage Isolera flash columnchromatography using 50% petroleum ether in EtOAc to get the tittlecompound. Yield: 38% (0.32 g, pale yellow solid). LCMS: (Method A) 166.1(M+H), Rt. 1.2 min, 58.7% (Max).

Step 2: 5-(chloromethyl)benzo[d]thiazole

To a stirred solution of benzo[d]thiazol-5-ylmethanol, Step 1: Example29, (0.3 g, 1.82 mmol) in dry DCM (3 mL), was added thionyl chloride(0.4 mL, 5.46 mmol) slowly at 0° C. The reaction mixture was stirred atRT for 1 h. The reaction mixture was then concentrated and the resultingcrude residue was co-distilled with DCM (3×10 mL) and dried under vacuumto give the tittle compound. Yield: 85% (0.28 g, pale yellow solid).LCMS: (Method A) 184.0 (M+H), Rt. 1.9 min, 94.1% (Max).

Example 29:5-((7-methoxy-2-methyl-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)methyl)benzo[d]thiazole

To a stirred solution of Intermediate 8 (0.12 g, 0.63 mmol) and TEA(0.22 mL, 1.57 mmol) in DMF (2 mL), was added5-(chloromethyl)benzo[d]thiazole, Step 2: Example 29, (0.13 g, 0.69mmol) at RT and the reaction mixture was stirred at RT for 48 h whilebeing monitored by TLC. After completion, the reaction mixture wasconcentrated under reduced pressure, the residue was suspended withwater (10 mL) and extracted with EtOAc (2×25 mL). The combined organiclayer was dried over Na₂SO₄ and concentrated. The resulting cruderesidue was purified first by Biotage Isolera using 1-2% MeOH in DCM aseluent, followed by prep-HPLC using method B to get the tittle compound.Yield: 48% (102 mg, off white solid). ¹H NMR (400 MHz, DMSO-d₆): δ 9.37(s, 1H), 8.10 (d, J=8.4 Hz, 1H), 8.05 (s, 1H), 7.52 (dd, J=8.0 Hz, 1.2Hz, 1H), 6.96 (d, J=8.4 Hz, 1H), 6.67-6.61 (m, 2H), 3.92 (d, J=18.0 Hz,1H), 3.84 (d, J=14.0 Hz, 1H), 3.70 (s, 3H), 3.24 (d, J=14.0 Hz, 1H),3.17-3.06 (m, 1H), 3.03-2.95 (m, 1H), 2.72-2.45 (m, 4H), 0.76 (d, J=6.4Hz, 3H). LCMS: (Method A) 339.2 (M+H), Rt. 1.6 min, 99.3% (Max). HPLC:(Method A) Rt. 3.3 min, 99.4% (Max), 98.7% (220 nm).

Example 30:7-methoxy-2-methyl-3-((2,3,4a,8a-tetrahydrobenzo[b][1,4]dioxin-6-yl)methyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Step 1: (2,3-dihydrobenzo[b][1,4]dioxin-6-yl)methanol

To a stirred solution of 2,3-dihydrobenzo[b][1,4]dioxine-6-carbaldehyde(1.0 g, 6.09 mmol) in MeOH (10 mL) was added NaBH₄ (0.28 g, 6.69 mmol)at 0□ and the reaction mixture was stirred for 1 h at RT. The reactionwas monitored by TLC and after completion, the reaction mixture wasdiluted with water (20 mL), and extracted with EtOAc (2×50 mL). Thecombined organic layer was dried over Na₂SO₄ and concentrated to affordthe tittle compound. Yield: 70% (0.71 g, colourless gummy solid). ¹H NMR(400 MHz, DMSO-d₆): δ 6.79-6.73 (m, 3H), 5.04 (t, J=5.6 Hz, 1H), 4.36(d, J=5.6 Hz, 2H), 4.23 (s, 4H). LCMS: (Method A) No ionisation (M+H),Rt. 1.3 min, 95.7% (Max).

Step 2: 6-(chloromethyl)-2,3-dihydrobenzo[b][1,4]dioxine

To a stirred solution of (2,3-dihydrobenzo[b][1,4]dioxin-6-yl)methanol,Step 1: Example 30, (0.3 g, 1.81 mmol) in dry DCM (3 mL), was addedthionyl chloride (0.4 mL, 5.42 mmol) slowly at 0° C. The reactionmixture was stirred at RT for 1 h. The reaction mixture wasconcentrated, and the resulting residue was co-distilled with DCM (3×10mL) and dried under vacuum to give the tittle compound. Yield: 95% (0.31g, colourless gummy solid). LCMS: (Method A) No ionisation (M+H), Rt.1.8 min, 82.3% (Max).

Example 30:3-((2,3-dihydrobenzo[b][1,4]dioxin-6-yl)methyl)-7-methoxy-2-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

To a stirred solution of Intermediate 8 (0.12 g, 0.63 mmol) and TEA(0.22 mL, 1.57 mmol) in DMF (2 mL), was added6-(chloromethyl)-2,3-dihydrobenzo[b][1,4]dioxine, Step 2: Example 30(0.13 g, 0.69 mmol) at RT and the reaction mixture was stirred at RT for48 h. After completion (TLC), the reaction mixture was concentratedunder reduced pressure. The residue was suspended in water (10 mL) andextracted with EtOAc (2×25 mL). The combined organic layer was driedover Na₂SO₄ and concentrated. The resulting crude material was purifiedby Isolera using 1-2% MeOH in DCM followed by Prep-HPLC using Method Bto get tittle compound. Yield: 32% (71 mg, pale brown gum). ¹H NMR (400MHz, DMSO-d₆): δ 6.94 (d, J=8.0 Hz, 1H), 6.82 (s, 1H), 6.78 (br s, 2H),6.67-6.60 (m, 2H), 4.21 (s, 4H), 3.70 (s, 3H), 3.64-3.50 (m, 2H), 3.17(d, J=14.0 Hz, 1H), 3.09-3.00 (m, 1H), 2.98-2.89 (m, 1H), 2.62-2.45 (m,4H), 0.69 (d, J=6.4 Hz, 3H). LCMS: (Method A) 340.3 (M+H), Rt. 1.7 min,99.5% (Max). HPLC: (Method A) Rt. 3.0 min, 98.6% (Max), 98.8% (220 nm).

Example 31:5-((7-methoxy-2-methyl-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)methyl)benzo[d]thiazole

Step 1: 2,3-dibromo-6-methoxypyridine

To a stirred solution of 2-bromo-6-methoxypyridine (10 g, 0.053 mol) indry ACN (100 mL), was added N-bromosuccinimide (18.82 g, 0.106 mol) atRT. The reaction mixture was stirred at 90□ for 16 h. The completion ofreaction was monitored by TLC. After completion, the reaction wasfiltered through a celite bed, diluted with water (30 mL) and exactedwith 10% EtOAc in petroleum ether (2×100 mL). The combined organic layerwashed with water (10 mL), brine (10 mL) dried over Na₂SO₄ andconcentrated. The resulting crude material was purified bycrystallization (5 mL DCM in 50 mL n-pentane). The solid was filtered,washed with n-pentane and then dried unber vacuum to get afford thetittle compound. Yield: 35% (4.92 g, off white solid). ¹H NMR (400 MHz,CDCl₃): δ 7.70 (d, J=8.4 Hz, 1H), 6.62 (d, J=8.4 Hz, 1H), 3.93 (s, 3H),LCMS: (Method A) 367.9 (M+H), Rt. 2.4 min, 96.7% (Max).

Step 2:4,4,5,5-tetramethyl-2-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-1,3,2-dioxaborolane

To a stirred solution of 2-(2-bromoethoxy)tetrahydro-2H-pyran (10 g,0.048 mol) in dry DMF (240 mL), were added bis(pinacolato)diboron (18.31g, 0.071 mol), polymer-bound PPh₃ (1.2 g, 0.004 mol), LiOMe (3.63 g,0.096 mol), CuI (0.91 g, 0.004 mol) at RT. The reaction mixture wasstirred at RT for overnight. Completion of the reaction was monitored byTLC. After completion, the mixture was filtered through a celite-bed andwashed with DCM (2×10 mL). The filtrate was poured into sat. NH₄Clsolution (50 mL) and exacted with EtOAc (3×100 mL). The combined organiclayer was washed with ice-cold water (2×50 mL), brine (50 mL), driedover Na₂SO₄ and concentrated under reduced pressure to get the titlecompound. Yield: 70% (8.5 g, colorless liquid). ¹H NMR: 1H-NMR (400 MHz,CDCl₃): δ 4.64 (t, J=4.0 Hz, 1H), 3.94-3.88 (m, 2H), 3.56-3.52 (m, 2H),1.90-1.75 (m, 1H), 1.73-1.65 (m, 1H), 1.61-1.52 (m, 4H), 1.28 (s, 12H),1.21 (t, J=8.0 Hz, 2H),

Step 3: Potassiumtrifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate

To a stirred solution of4,4,5,5-tetramethyl-2-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-1,3,2-dioxaborolane,Step 2: Example 31, (6 g, 23.44 mmol) in dry THF (90 mL), was added sat.aq. KHF₂ solution (5.72 g, 73.33 mmol) at RT, and the mixture wasstirred at RT for 2 h. Then the reaction mixture was concentrated. Theresulting gum was washed with dry acetone (4×60 mL), filtered andconcentrated under reduced pressure. The residue was dissolved in dryacetone (20 mL), cooled to 0° C., and diethyl ether was added until asmall amount of precipitate formed. The suspension was stirred at 0□ for30 min and filtered. The solid was washed with diethyl ether (20 mL) toafford the tittle compound. Yield: 74% (4.1 g, white solid). ¹H NMR:(400 MHz, DMSO-d₆): δ 4.43 (t, J=4.0 Hz, 1H), 3.74-3.71 (m, 1H),3.61-3.54 (m, 1H), 3.36-3.26 (m, 1H), 3.25-3.21 (m, 1H), 1.71-1.66 (m,1H), 1.58-1.51 (m, 1H), 1.45-1.36 (m, 4H), 0.38-0.24 (m, 2H),

Step 4:6-methoxy-2,3-bis(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)pyridine

To a stirred solution of 2,3-dibromo-6-methoxypyridine, Step 1: Example31, (1.4 g, 5.30 mmol), potassiumtrifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate, Step 3: Example31, (3.7 g, 15.90 mmol) and cataCXium®A (0.35 g, 1.06 mmol) in dry 1,4dioxane (12 mL), was added a solution of cesium carbonate (1.62 g, 31.80mmol) in water (4 mL) at RT. The reaction mixture was degassed for 10min using N₂ gas. Then Pd(OAc)₂ (0.33 g, 1.59 mmol) was added at RT andthe reaction mixture was heated to 100□ for 20 h. Completion of thereaction was monitored by TLC. After completion, the reaction mixturewas diluted with EtOAc (10 mL) and brine (10 mL) and the aqueous layerwas extracted with EtOAc (2×20 mL), washed with water (10 mL), brine (10mL), dried over Na₂SO₄ and concentrated under reduced pressure. Theresulting crude material was purified by flash chromatography using12-15% EtOAc in petroleum ether to afford the tittle compound. Yield:57% (1.1 g, brown gummy solid). ¹H NMR (400 MHz, CDCl₃): δ 7.40 (d,J=8.4 Hz, 1H), 6.53 (d, J=8.0 Hz, 1H), 4.62 (d, J=20.8 Hz, 2H),4.20-4.11 (m, 1H), 3.95-3.89 (m, 2H), 3.88 (s, 3H), 3.81-3.70 (m, 2H),3.61-3.51 (m, 1H), 3.50-3.46 (m, 2H), 3.07 (t, J=7.2 Hz, 2H), 2.91 (t,J=7.2 Hz, 2H), 1.81 (t, J=8.4 Hz, 2H), 1.71 (t, J=10.0 Hz, 2H),1.62-1.59 (m, 8H). LCMS: (Method A) 366.2 (M+H), 1.7 min, 90.1% (Max).

Step 5: 2,2′-(6-methoxypyridine-2,3-diyl)bis(ethan-1-ol)

To a stirred solution of6-methoxy-2,3-bis(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)pyridine, Step4: Example 31, (1.1 g, 3.01 mmol) in dry MeOH (12 mL) was addedp-TsOH.H₂O (1.31 g, 6.93 mmol) at 0° C. and the reaction mixture wasstirred at RT for overnight. Completion of the reaction was monitored byTLC. After completion, the reaction mixture was concentrated, dilutedwith sat. aq. NaHCO₃ solution (10 mL) and extracted with DCM (2×20 mL).The combined organic layer was washed with water (5 mL), brine (5 mL),dried over Na₂SO₄ and concentrated under reduced pressure. The resultingcrude residue was taken for next step without further purification.Yield: 55% (325 mg, yellow gummy solid). ¹H NMR (400 MHz, DMSO-d₆): δ7.47 (d, J=2.4 Hz, 1H), 6.65 (d, J=3.2 Hz, 1H), 4.09 (t, J=4.8 Hz, 2H),3.93 (s, 3H), 3.84 (t, J=3.6 Hz, 2H), 3.00 (t, J=5.6 Hz, 2H), 2.85 (t,J=3.6 Hz, 2H). LCMS: (Method A) 198.1 (M+H), 0.5 min, 82.6% (Max).

Step 6: (6-methoxypyridine-2,3-diyl)bis(ethane-2,1-diyl)dimethanesulfonate

To a stirred solution of2,2′-(6-methoxypyridine-2,3-diyl)bis(ethan-1-ol), Step 5: Example 31,(320 mg, 1.63 mmol) in dry DCM (4 mL), were added TEA (0.68 mL, 4.89mmol) and mesyl chloride (0.29 mL, 4.08 mmol) at 0□ and the reactionmixture was stirred at RT for 30 min. Completion of the reaction wasmonitored by TLC. After completion, the reaction mixture wasconcentrated, diluted with sat. aq. NaHCO₃ solution (3 mL) and extractedwith DCM (2×20 mL). The combined organic layer was washed with water (3mL), brine (3 mL), dried over Na₂SO₄ and concentrated under reducedpressure. The resulting crude residue was taken for next step withoutany purification. Yield: 87% (500 mg, yellow gummy solid). ¹H NMR (400MHz, DMSO-d₆): δ 7.42 (d, J=8.4 Hz, 1H), 6.62 (d, J=8.4 Hz, 1H), 4.75(t, J=3.6 Hz, 2H), 4.36 (t, J=7.2 Hz, 2H), 3.91 (s, 3H), 3.18 (t, J=6.8Hz, 2H), 3.04 (t, J=6.8 Hz, 2H), 2.95 (s, 3H), 2.94 (s, 3H). LCMS:(Method A) 354.0 (M+H), 1.6 min, 85.4% (Max).

Step 7: 7-benzyl-2-methoxy-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine

To a stirred solution of(6-methoxypyridine-2,3-diyl)bis(ethane-2,1-diyl) dimethanesulfonate,Step 6: Example 31, (500 mg, 1.14 mmol) in dry dichloroethane (2.5 mL)was added benzyl amine (1.5 mL, 14.16 mmol) at RT. The reaction mixturewas stirred for 16 h at 50□. The completion of reaction was monitored byTLC. After completion, the reaction mixture was diluted with DCM (10mL), washed with sat. aq. NaHCO₃ solution (3×3 mL), brine (2 mL), driedover Na₂SO₄ and concentrated. The resulting crude residue was purifiedby flash chromatography using 70-90% EtOAc in petroleum ether to get thetittle compound. Yield: 78%, (300 mg, yellow liquid). LCMS: (Method A)269.2 (M+H), Rt.1.2 min, 48.1% (Max).

Step 8: 2-methoxy-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine

To a stirred solution of7-benzyl-2-methoxy-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine, Step 7:Example 31, (300 mg, 1.19 mmol) in dry MeOH (2.5 mL), was added Pd—C (30mg, 10 wt %) at RT and the reaction mixture was degassed with H₂ gas.The reaction mixture was stirred under H₂ pressure (4 kg/cm²) for 16 hat 50□. The completion of reaction was monitored by LCMS. Aftercompletion, the reaction mixture was filtered through a celite-bed andconcentrated to obtain the crude title compound which was used in thenext step directly. Yield: 69% (140 mg, colorless liquid). LCMS: (MethodA) 179.1 (M+H), Rt.0.4 min, 70.2% (Max).

Step 9:5-(1-(2-methoxy-5,6,8,9-tetrahydro-7H-pyrido[2,3-d]azepin-7-yl)ethyl)benzo[d]thiazole

To a stirred solution of 52-methoxy-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine, Step 8: Example31, (130 mg, 0.73 mmol) in dry DMF (2 mL), was added TEA (0.15 mL, 1.09mmol) and the reaction mixture was stirred for 10 min at RT.5-(1-chloroethyl)benzo[d]thiazole, Intermediate 2, (172 mg, 0.87 mmol),was added and the reaction mixture was stirred for 16 h at 80□.Completion of the reaction was monitored by LCMS. After completion, thereaction mixture was concentrated, diluted with water (2 mL) andextracted with DCM (3×10 mL). The combined organic layer washed withwater (5 mL), brine (5 mL), dried over Na₂SO₄ and concentrated. Theresulting crude residue was purified by Prep-HPLC (method B) to affordthe tittle compound. Yield: 5% (13 mg, white solid). ¹H NMR (400 MHz,DMSO-d₆): δ 9.36 (s, 1H), 8.09 (d, J=8.4 Hz, 1H), 8.03 (s, 1H), 7.54 (d,J=8.0 Hz, 1H), 7.37 (d, J=8.4 Hz, 1H), 6.48 (d, J=8.0 Hz, 1H), 4.07 (q,J=6.4 Hz, 1H), 3.76 (s, 3H), 2.93 (t, J=4.0 Hz, 2H), 2.76 (t, J=3.6 Hz,2H), 2.69-2.55 (m, 4H), 1.42 (d, J=6.8 Hz, 3H). LCMS: (Method A) 340.1(M+H), Rt.1.3 min, 98.1% (Max). HPLC: (Method B) Rt. 5.6 min, 98.4%(Max), 97.3% (220 nm).

Example 32:5-(1-(7-(pyridin-2-yl)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

Step 1:3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yltrifluoromethanesulfonate

To a stirred solution of3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol,Example 33, (200 mg, 0.61 mmol) in DCM at 0° C. were addedtrifluoromethanesulfonic anhydride (0.35 mL, 0.92 mmol) and TEA (0.26mL, 1.85 mmol) and the reaction mixture was stirred at RT for 1 h. Aftercompletion (TLC), the reaction mixture was quenched with aq. NaHCO₃(10%, 50 mL) and extracted with DCM (2×50 mL). The combined organiclayer was dried over Na₂SO₄ and concentrated. The resulting cruderesidue was purified by Biotage Isolera column chromatography using 50%EtOAc in petroleum ether to afford the tittle compound. Yield: 29% (82mg, brown gum). LCMS: (Method A) 457.0 (M+H), Rt. 1.8 min, 69.4% (Max).

Step 2:5-(1-(7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

A solution of3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yltrifluoromethanesulfonate, Step 1: Example 32, (80 mg, 0.17 mmol) in1,4-dioxane (0.8 mL) was degassed with nitrogen for 10 min. KOAc (52 mg,0.52 mmol), bis(pinacolato)diboron (67 mg, 0.26 mmol) and[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complexwith dichloromethane (8 mg, 0.01 mmol) were added and the reactionmixture was stirred for overnight at 100° C. After completion (TLC), thereaction mixture was filtered through a celite pad and the filtrate wasconcentrated. This residue was diluted with water and extracted with DCM(2×30 mL). The combined organic layer was dried over Na₂SO₄ andconcentrated to afford the tittle compound. Yield: 76% (120 mg, browngum). LCMS: (Method A) 435.2 (M+H), Rt. 1.9 min, 53.5% (Max).

Example 32:5-(1-(7-(pyridin-2-yl)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole

A stirred solution of5-(1-(7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)benzo[d]thiazole,Step 2: Example 32, (120 mg, 0.27 mmol) in 1,4-dioxane (0.96 mL) andwater (0.24 mL) was degassed with nitrogen for 10 min. Cs₂CO₃ (270 mg,0.82 mmol), 2-chloropyridine (34 mg, 0.30 mmol) and Pd(PPh₃)₄ (32 mg,0.02 mmol) were added and the reaction mixture was stirred for overnightat 90° C. After completion (TLC), the reaction mixture was filteredthrough a celite-pad and the filtrate was concentrated. The residue wasdiluted water and extracted with DCM (2×50 mL). The combined organiclayer was dried over Na₂SO₄ and concentrated. The resulting cruderesidue was purified by prep-HPLC (method A) to afford the titlecompound. Yield: 10% (6 mg, pale yellow gum). ¹H NMR (400 MHz, DMSO-d₆):δ 9.37 (s, 1H), 8.61 (d, J=4.4 Hz, 1H), 8.10 (d, J=8.4 Hz, 1H), 8.05 (s,1H), 7.90-7.76 (m, 4H), 7.56 (d, J=9.6 Hz, 1H), 7.32-7.28 (m, 1H), 7.18(d, J=8.4 Hz, 1H), 4.10 (q, J=6.8 Hz, 1H), 2.97-2.88 (m, 4H), 2.68-2.52(m, 4H), 1.44 (d, J=6.8 Hz, 3H), LCMS: (Method A) 386.1 (M+H), Rt. 1.1min, 99.1% (Max). HPLC: (Method A) Rt. 2.1 min, 99.0% (Max), 99.1% (220nm).

Example 33:3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol

Step 1: 2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol hydrobromide

A solution of 7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine,Intermediate 6, (1.1 g, 9.93 mmol) in aq. HBr (48%, 3.3 mL) was stirredat 65° C. for overnight. After completion (TLC), the reaction mixturewas concentrated under reduced pressure. The resulting solid wastriturated with hexane-diethyl ether (8:2) to give the title compound.Yield: 75% (0.6 g, brown gum). ¹H NMR (400 MHz, DMSO-d₆): δ 6.98 (d,J=8.0 Hz, 1H), 6.62-6.54 (m, 2H), 3.17-3.12 (m, 4H), 2.98-2.95 (m, 4H).LCMS: (Method A) 164.2 (M+H), Rt. 0.7 min, 69.4% (Max).

Example 33:3-(1-(benzo[d]thiazol-5-yl)ethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol

To a stirred solution of 2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol (300mg, 1.83 mmol, Step 1: Example 33) in dry DMF (3 mL), were added TEA(0.76 mL, 5.45 mmol) and 5-(1-chloroethyl)benzo[d]thiazole, Intermediate2, (430 mg, 2.17 mmol) at RT and the reaction mixture was stirred at 70°C. for overnight. After completion (TLC), and the reaction mixture wasconcentrated at 50° C. under reduced pressure. The residue was suspendedwith water (10 mL) and extracted with EtOAc (2×100 mL). The combinedorganic layer was dried over Na₂SO₄ and concentrated. The crude residuewas purified by Biotage Isolera using 2-3% MeOH in DCM to afford thetitle compound. Yield: 29% (170 mg, pale brown gum). LCMS: (Method A)325.0 (M+H), Rt. 1.9 min, 59.5% (Max).

Portion of this material (70 mg) was further purified by Prep-HPLC(Method B) to obtain the title compound. Yield: 32 mg, pale yellowsolid. ¹H NMR (400 MHz, DMSO-d₆): δ 9.36 (s, 1H), 9.01 (s, 1H), 8.08 (d,J=8.4 Hz, 1H), 8.01 (s, 1H), 7.52 (d, J=8.4 Hz, 1H), 6.81 (d, J=8.0 Hz,1H), 6.46 (s, 1H), 6.41 (d, J=8.0 Hz, 1H), 4.03 (q, J=6.8 Hz, 1H),2.71-2.67 (m, 4H), 2.56-2.50 (m, 4H), 1.40 (d, J=6.40 Hz, 3H). LCMS:(Method A) 325.1 (M+H), Rt. 1.3 min, 98.7% (Max). HPLC: (Method A) Rt.2.41 min, 98.7% (Max), 98.6% (220 nm).

Example 34:6-(1-(7-methoxy-1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)ethyl)-2,3-dihydrofuro[3,2-b]pyridine

To a stirred solution of6-(1-chloroethyl)-2,3-dihydrofuro[3,2-b]pyridine, Intermediate 9, (120mg, 0.65 mmol) in dry DMF (1.2 mL) were added7-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine, Intermediate 6, (127mg, 0.59 mmol) and TEA (0.25 mL, 3.26 mmol) and the reaction mixture washeated to 80° C. overnight. After completion, the reaction mixture wasconcentrated under vacuum. The residue was diluted with water andextracted with EtOAc (2×40 mL). The combined organic layer was washedwith water (10 mL), dried over Na₂SO₄ and concentrated. The cruderesidue was purified by flash column chromatography using 50-60% EtOAcin petroleum ether as eluent to get the title compound. Yield: 29%(0.048 g, pale brown gum). ¹H NMR (400 MHz, DMSO-d₆): δ 7.93 (s, 1H),7.09 (s, 1H), 6.96 (d, J=8.4 Hz, 1H), 6.66 (d, J=2.4 Hz, 1H), 6.66 (dd,J=8.0 Hz, 2.4 Hz, 1H), 4.61 (t, J=8.8 Hz, 2H), 3.87 (q, J=7.2 Hz, 1H),3.68 (s, 3H), 3.20 (t, J=8.8 Hz, 2H), 2.82-2.72 (m, 4H), 2.62-2.35 (m,4H), 1.32 (d, J=6.8 Hz, 3H). LCMS: (Method A) 325.2 (M+H), Rt. 1.3 min,96.7% (Max). HPLC: (Method A) Rt. 2.4 min, 96.6% (Max), 96.6% (220 nm).

The examples below were synthesized according to procedures described inthe previous examples. These compounds and their tautomers, enantiomers,and salts are further preferred embodiments of the present invention.

Con- figura- Opti- tion cal speci- rota- fica- No Structure tion tion 1HNMR 28

Racemic 1H NMR (400 MHz, DMSO-d6): δ 8.06 (d, J = 8.0 Hz, 1H), 8.00 (s,1H), 7.79 (d, J = 8.8 Hz, 1H), 6.98 (d, J = 8.0 Hz, 1H), 6.68-6.64 (m,2H), 4.00-3.87 (m, 2H), 3.61 (s, 3H), 3.28-3.24 (m, 1H), 3.16-3.13 (m,1H), 3.02-2.99 (m, 1H), 2.72-2.62 (m, 2H), 2.60-2.51 (m, 2H), 0.79 (d, J= 6.8 Hz, 3H). 29

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.10 (d, J = 8.4 Hz,1H), 8.05 (s, 1H), 7.52 (dd, J = 8.0 Hz, 1.2 Hz, 1H), 6.96 (d, J = 8.4Hz, 1H), 6.67-6.61 (m, 2H), 3.92 (d, J = 18.0 Hz, 1H), 3.84 (d, J = 14.0Hz, 1H), 3.70 (s, 3H), 3.24 (d, J = 14.0 Hz, 1H), 3.17-3.06 (m, 1H),3.03-2.95 (m, 1H), 2.72-2.45 (m, 4H), 0.76 (d, J = 6.4 Hz, 3H). 30

Racemic 1H NMR (400 MHz, DMSO-d6): δ 6.94 (d, J = 8.0 Hz, 1H), 6.82 (s,1H), 6.78 (br s, 2H), 6.67-6.60 (m, 2H), 4.21 (s, 4H), 3.70 (s, 3H),3.64-3.50 (m, 2H), 3.17 (d, J = 14.0 Hz, 1H), 3.09-3.00 (m, 1H),2.98-2.89 (m, 1H), 2.62-2.45 (m, 4H), 0.69 (d, J = 6.4 Hz, 3H). 37

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.10 (d, J = 8.3 Hz,1H), 8.04 (s, 1H), 7.62 (t, J = 3.4 Hz, 2H), 7.54 (d, J = 8.2 Hz, 1H),7.29 (d, J = 7.8 Hz, 1H), 4.10-4.05 (m, 2H), 3.00 (s, 3H), 2.95-2.86 (m,4H), 2.68-2.63 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H). 43

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.76 (s, 1H), 9.37 (s, 1H), 8.09(d, J = 8.4 Hz, 1H), 8.03 (s, 1H), 7.54 (d, J = 8.4 Hz, 1H), 7.27-7.24(m, 2H), 6.96 (d, J = 8.4 Hz, 1H), 4.06 (q, J = 6.0 Hz, 1H), 2.78 (br s,4H), 2.65-2.48 (m, 4H), 1.99 (s, 3H), 1.42 (d, J = 6.4 Hz, 3H). 51

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.38 (s, 1H), 8.71 (d, J = 2.0 Hz,1H), 8.11 (d, J = 8.0 Hz, 1H), 8.05-8.03 (m, 2H), 7.55 (d, J = 8.0 Hz,1H), 4.12 (q, J = 6.4 Hz, 1H), 3.26 (s, 3H), 3.19-3.16 (m, 2H),3.01-2.95 (m, 2H), 2.75-2.58 (m, 4H), 1.44 (d, J = 6.8 Hz, 3H). 52

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.68 (s, 1H), 8.09(d, J = 8.0 Hz, 1H), 8.04 (s, 1H), 7.97 (s, 1H), 7.54 (d, J = 8.4 Hz,1H), 4.35 (s, 1H), 4.10 (q, J = 6.4 Hz, 1H), 3.19-3.11 (m, 2H), 3.08 (s,3H), 2.99-2.94 (m, 2H), 2.75-2.54 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H). 60

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.38 (s, 1H), 8.28 (d, J = 5.6 Hz,1H), 8.10 (d, J = 8.4 Hz, 1H), 8.04 (s, 1H), 7.54 (d, J = 8.0 Hz, 1H),7.16 (d, J = 8.4 Hz, 1H), 6.89 (d, J = 2.4 Hz, 1H), 6.83 (dd, J = 2.4,8.0 Hz, 1H), 6.74 (d, J = 2.0 Hz, 1H), 6.65 (dd, J = 2.4, 5.6 Hz, 1H),4.09 (q, J = 6.8 Hz, 1H), 2.92-2.81 (m, 4H), 2.67-2.55 (m, 4H), 2.38 (s,3H), 1.44 (d, J = 6.4 Hz, 3H). 62

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.10 (d, J = 8.4 Hz,1H), 8.04 (s, 1H), 7.56-7.53 (d, J = 7.2 Hz, 1H), 7.13 (d, J = 8.0 Hz,1H), 6.90-6.84 (m, 2H), 6.62 (s, 1H), 4.10-4.06 (m, 1H), 2.88-2.82 (m,4H), 2.68-2.52 (m, 4H), 2.38 (s, 3H), 2.35 (s, 3H), 1.44 (d, J = 6.8 Hz,3H). 92

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.98 (s, 1H), 9.38 (s, 1H), 8.34(d, J = 2.0 Hz, 1H), 8.10 (d, J = 8.4 Hz, 1H), 8.05 (s, 1H), 7.72 (d, J= 2.0 Hz, 1H), 7.55 (d, J = 8.4 Hz, 1H), 4.12-4.05 (m, 1H), 3.00-2.96(m, 2H), 2.86-2.77 (m, 2H), 2.68-2.65 (m, 2H), 2.59-2.54 (m, 2H), 2.03(s, 3H), 1.42 (d, J = 6.8 Hz, 3H). 98

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.38 (s, 1H), 9.04 (d, J = 2.4 Hz,1H), 8.35 (d, J = 2.4 Hz, 1H), 8.11 (d, J = 8.4 Hz, 1H), 8.05 (s, 1H),7.54 (d, J = 9.2 Hz, 1H), 4.12 (q, J = 6.8 Hz, 1H), 3.25-3.16 (m, 2H),3.06-2.98 (m, 2H), 2.76-2.54 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H), 99

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.74 (br s, 1H), 9.36 (s, 1H),8.10-8.03 (m, 3H), 7.54 (d, J = 8.0 Hz, 1H), 7.30 (d, J = 1.6 Hz, 1H),4.10-4.05 (m, 1H), 3.02-2.95 (m, 2H), 2.97 (s, 3H), 2.84-2.76 (m, 2H),2.65-2.56 (m, 4H), 1.42 (d, J = 6.8 Hz, 3H). 106

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.39 (d, J = 1.6 Hz, 1H), 9.12 (s,1H), 8.15-8.10 (m, 2H), 8.00 (s, 1H), 7.47 (d, J = 8.4 Hz, 1H), 4.12 (d,J = 14.8 Hz, 1H), 3.88 (q, J = 6.0 Hz, 1H), 3.79 (d, J = 15.2 Hz, 1H),3.25-3.10 (m, 3H), 3.09-2.98 (m, 1H), 1.74-1.72 (m, 2H), 3.00 (d, J =6.0 Hz, 3H). 107

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.83 (s, 1H), 9.37 (s, 1H), 8.09(d, J = 8.8 Hz, 1H), 7.93 (s, 1H), 7.46-7.42 (m, 1H), 7.36 (d,J = 2.0Hz, 1H, 7.27 (dd, J = 2.0, 8.0 Hz, 1H), 6.75 (d, J = 8.0 Hz, 1H), 3.90(d, J = 14.4 Hz, 1H), 3.73 (q, J = 6.8 Hz, 1H), 3.64 (d, J = 14.4 Hz,1H), 3.13- 3.03 (m, 1H), 2.98-2.92 (m, 1H), 2.84-2.77 (m, 2H), 2.03 (s,3H), 1.70-1.52 (m, 2H), 1.33 (d, J = 6.8 Hz, 3H). 108

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.30 (s, 1H), 8.03 (d, J = 8.4 Hz,1H), 7.97 (s, 1H), 7.80 (s, 1H), 7.48 (dd, J = 1.6, 8.2 Hz, 1H), 6.19(s, 2H), 4.03 (q, J = 6.4 Hz, 1H), 2.72-1.67 (m, 2H), 2.62-2.45 (m, 6H),1.34 (d, J = 6.8 Hz, 3H). 109

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.10 (d, J = 8.4 Hz,1H), 8.04-8.03 (m, 2H), 7.76 (s, 1H), 7.55 (d, J = 8.4 Hz, 1H),7.27-7.22 (m, 2H), 7.03 (d, J = 7.6 Hz, 1H), 4.09-4.07 (m, 1H), 3.83 (s,3H), 2.87-2.80 (m, 4H), 2.68-2.52 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H). 110

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.38 (s, 1H), 8.11-8.08 (m, 2H),7.95 (s, 1H), 7.83 (s, 1H), 7.46 (d, J = 8.0 Hz, 1H), 7.39 (s, 1H), 7.25(d, J = 7.6 Hz, 1H), 6.81 (d, J = 6.8 Hz, 1H), 3.93 (d, J = 14.4 Hz,1H), 3.86 (s, 3H), 3.78 (q, J = 6.4 Hz, 1H), 3.67 (d, J = 14.8 Hz, 1H),3.18-3.09 (m, 1H), 3.01-2.96 (m, 1H), 2.88 (t, J = 4.8 Hz, 2H),1.73-1.58 (m, 2H), 1.35 (d, J = 6.4 Hz, 3H). 111

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.09 (d, J = 8.4 Hz,1H), 8.03 (s, 1H), 7.54 (d, J = 8.4 Hz, 1H), 7.02-6.94 (m, 3H), 4.06 (t,J = 6.4 Hz, 1H), 2.81-2.80 (m, 4H), 2.68-2.60 (m, 4H), 2.41 (s, 3H),1.42 (d, J = 6.8 Hz, 3H). 112

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.38 (s, 1H), 8.09 (d, J = 8.4 Hz,1H), 7.94 (s, 1H), 7.45 (d, J = 8.4 Hz, 1H), 7.09 (s, 1H), 6.96 (t, J =2.0 Hz, 1H), 6.79 (d, J = 6.8 Hz, 1H), 3.91 (d, J = 14.8 Hz, 1H),3.78-3.72 (m, 1H), 3.64 (d, J = 14.4 Hz, 1H), 3.09 (br s, 1H), 3.00-2.92(m, 1H), 2.84 (br s, 2H), 2.46 (s, 3H), 1.72-1.53 (m, 2H), 1.34 (d, J =6.4 Hz, 3H). 113

1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.10 (d, J = 8.4 Hz, 1H),8.04 (s, 1H), 7.63-7.60 (m, 2H), 7.54 (d, J = 8.0 Hz, 1H), 7.29 (d, J =8.0 Hz, 1H), 4.12-4.05 (m, 2H), 3.00 (s, 3H), 2.95-2.86 (m, 4H),2.68-2.53 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H). 114

1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.10 (d, J = 8.0 Hz, 1H),8.04 (s, 1H), 7.63-7.60 (m, 2H), 7.54 (d, J = 8.4 Hz, 1H), 7.29 (d, J =8.0 Hz, 1H), 4.12-4.05 (m, 2H), 3.00 (s, 3H), 2.95-2.86 (m, 4H),2.68-2.53 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H). 115

1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.10 (d, J = 8.4 Hz, 1H),8.04 (s, 1H), 7.63-7.60 (m, 2H), 7.54 (d, J = 8.4 Hz, 1H), 7.29 (d, J =7.6 Hz, 1H), 4.12-4.05 (m, 2H), 3.00 (s, 3H), 2.95-2.86 (m, 4H),2.68-2.53 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H). 116

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.11-8.01 (m, 2H),7.55-7.50 (m, 1H), 7.30-7.26 (m, 1H), 6.70-6.63 (m, 2H), 5.26-5.18 (m,1H), 4.72-4.66 (m, 1H), 4.12-4.05 (m, 1H), 3.73-3.67 (m, 3H), 3.05-2.72(m, 4H), 2.21-2.13 (m, 2H), 1.45-1.40 (m, 3H). 117

Racemic 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.09 (d, J = 8.4 Hz,1H), 8.04 (s, 1H), 7.56-7.53 (m, 2H), 6.63 (d, J = 2.4 Hz, 1H), 4.97 (brs, 2H), 4.05 (q, J = 6.8 Hz, 1H), 2.89-2.85 (m, 2H), 2.79-2.65 (m, 2H),2.59-2.52 (m, 4H), 1.41 (d, J = 6.8 Hz, 3H). 118

1H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.08 (d, J = 8.4 Hz, 1H),8.02 (s, 1H), 7.52 (d, J = 8.4 Hz, 1H), 7.02-6.94 (m, 3H), 4.06 (q, J =6.8 Hz, 1H), 2.83-2.73 (m, 4H), 2.62-2.45 (m, 4H), 2.40 (s, 3H), 1.42(d, J = 6.8 Hz, 3H). 119

1H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.08 (d, J = 8.4 Hz, 1H),8.02 (s, 1H), 7.52 (d, J = 8.4 Hz, 1H), 7.02-6.94 (m, 3H), 4.06 (q, J =6.8 Hz, 1H), 2.83-2.73 (m, 4H), 2.62-2.45 (m, 4H), 2.40 (s, 3H), 1.42(d, J = 6.8 Hz, 3H). 120

Racemic 1H NMR (400 MHz, CD3OD): δ 9.25 (s, 1H), 8.13-8.03 (m, 3H), 7.62(dd, J = 1.6, 8.4 Hz, 1H), 7.50 (d, J = 2.4 Hz, 1H), 4.11 (q, J = 6.8Hz, 1H), 3.17-3.12 (m, 2H), 2.95-2.91 (m, 2H), 2.82-2.71 (m, 4H),2.58-2.53 (m, 1H), 1.53 (d, J = 6.8 Hz, 3H), 1.04-0.95 (m, 4H). 121

Racemic 1H NMR (400 MHz, CD3OD): δ 9.26 (s, 1H), 8.20 (d, J = 2.4 Hz,1H), 8.07-8.01 (m, 2H), 7.54-7.51 (m, 1H), 7.16-7.15 (s, 1H), 4.01 (d, J= 14.8 Hz, 1H), 3.86 (q, J = 6.4 Hz, 1H), 3.77 (d, J = 14.8 Hz, 1H),3.31-3.13 (m, 4H), 2.56-2.52 (m, 1H), 1.87-1.82 (m, 2H), 1.47 (d, J =6.4 Hz, 3H), 1.02-0.96 (m, 4H). 122

Racemic 1H NMR (400 MHz, DMSO-d6): δ 11.89 (s, 1H), 7.16-7.12 (m, 5H),4.26-4.15 (m, 1H), 3.59-3.51 (m, 1H), 3.18-3.08 (m, 1H), 3.01-2.88 (m,4H), 2.11 (s, 3H), 1.65-1.50 (m, 2H), 1.47 (d, J = 6.8 Hz, 3H).

Example B01: Human O-GlcNAcase Enzyme Inhibition Assay

5 μl of the appropriate concentration of a solution of inhibitor inMcIlvaine's Buffer (pH 6.5) in 2% DMSO (for a dose response curvecalculation) is added into each well of a 384-well plate (Greiner,781900). Then, 20 nM of His-Tagged hOGA and 10 μM of FL-GlcNAc(Fluorescein mono-beta-D-(2-deoxy-2-N-acetyl) glucopyranoside; MarkerGene Technologies Inc, M1485) were added to the 384-well plate for afinal volume of 20 μl. After incubation for 60 min at room temperature,the reaction was terminated by the addition of 10 μL of stop buffer (200mM glycine, pH 10.75). The level of fluorescence (Δ_(exc) 485 nm;(Δ_(emm) 520 nm) was read on a PHERAstar machine. The amount offluorescence measured was plotted against the concentration of inhibitorto produce a sigmoidal dose response curve to calculate an IC₅₀. Allindividual data was corrected by subtraction of the background (Thiamet3 uM=100% inhibition) whilst 0.5% DMSO was considered as the controlvalue (no inhibition).

Example B02: Pharmacodynamic Model: Total Protein O-GlcNAcylationImmunoassay (RL2 mAb, Meso Scale Electrochemiluminescence (ECL) Assay)

The test compound was administered orally to C57BL/6J mice. At definedtime intervals after compound administration, typically a time rangingbetween 2 and 48 hours, preferably between 4 and 24 hours, mice weresacrificed by decapitation for blood collection and forebraindissection. Right brain hemispheres were placed in 2 ml Precellys tubes,snap frozen in dry ice and stored at −80° C. Left hemispheres wereplaced in 2 ml Eppendorf tubes, snap frozen in dry ice and stored at−80° C. until further processing. Blood samples were collected inSarstedt tubes containing 35 IU of Heparin and kept at 4° C. Aftercentrifugation for 10 min at 3800×g, 4° C., 50 μL of plasma from eachsample was transferred to a 1.5 ml Eppendorf tube and stored at −80° C.

For the preparation of soluble brain protein for the immunoassay thehemispheres were homogenized in ice-cold Cytobuster reagent (71009-MerckMillipore) buffer with protease inhibitor cocktail. After centrifugationfor 15 min at 17000×g at 4° C. the supernatants were transferred intopolycarbonate tubes (1 ml). The supernatants were cleared bycentrifugation for 1 h. at 100000×g, 4° C., and the proteinconcentrations were determined by using the BCA kit (23227—Pierce,Rockford, Ill.) according to the manufacturer's instructions.

Total Protein O-GlcNAcylation Immunoassay:

Samples were randomised and 120 μg/ml (25 μl/well) of soluble brainprotein was directly coated on a Multi-array 96-well high bind plate(L15XB-3 High bind—Meso Scale Discovery) overnight at 4° C. Afterwashing (3× with PBS-T buffer), the plate was blocked with MSD blocker Asolution for 1 h. at room temperature (RT) under agitation. Afterwashing (3× with PBS-T buffer), the plate was incubated with 0.1 μg/mlof a mouse monoclonal antibody directed against O-GlcNAc moieties (RL2;MA1-072—Thermo Scientific) for 1 h. at RT under agitation. For the ECLassay, after washing (3× with PBS-T buffer), 1 μg/ml of a SULFO-TAG™labeled anti-mouse secondary antibody (Meso Scale Discovery) was addedand the plate was incubated for 1 h. at RT under agitation and protectedfrom light. After washing (3× with PBS-T buffer), 150 μl/well of 1× ReadBuffer T was added to the plates before reading on a Sector Imager 6000(Meso Scale Discovery).

Example B03: Pharmaceutical Preparations

(A) Injection vials: A solution of 100 g of an active ingredientaccording to the invention and 5 g of disodium hydrogen phosphate in 3 lof bi-distilled water was adjusted to pH 6.5 using 2 N hydrochloricacid, sterile filtered, transferred into injection vials, lyophilizedunder sterile conditions and sealed under sterile conditions. Eachinjection vial contained 5 mg of active ingredient.

(B) Suppositories: A mixture of 20 g of an active ingredient accordingto the invention was melted with 100 g of soy lecithin and 1400 g ofcocoa butter, poured into moulds and allowed to cool. Each suppositorycontained 20 mg of active ingredient.

(C) Solution: A solution was prepared from 1 g of an active ingredientaccording to the invention, 9.38 g of NaH₂PO₄.2 H₂O, 28.48 g ofNa₂HPO₄.12 H₂O and 0.1 g of benzalkonium chloride in 940 ml ofbi-distilled water. The pH was adjusted to 6.8, and the solution wasmade up to 1 l and sterilized by irradiation. This solution could beused in the form of eye drops.

(D) Ointment: 500 mg of an active ingredient according to the inventionwere mixed with 99.5 g of Vaseline under aseptic conditions.

(E) Tablets: A mixture of 1 kg of an active ingredient according to theinvention, 4 kg of lactose, 1.2 kg of potato starch, 0.2 kg of talc and0.1 kg of magnesium stearate was pressed to give tablets in aconventional manner in such a way that each tablet contained 10 mg ofactive ingredient.

(F) Coated tablets: Tablets were pressed analogously to EXAMPLE E andsubsequently coated in a conventional manner with a coating of sucrose,potato starch, talc, tragacanth and dye.

(G) Capsules: 2 kg of an active ingredient according to the inventionwere introduced into hard gelatin capsules in a conventional manner insuch a way that each capsule contained 20 mg of the active ingredient.

(H) Ampoules: A solution of 1 kg of an active ingredient according tothe invention in 60 l of bi-distilled water was sterile filtered,transferred into ampoules, lyophilized under sterile conditions andsealed under sterile conditions. Each ampoule contained 10 mg of activeingredient.

(I′) or (I) Inhalation spray: 14 g of an active ingredient according tothe invention were dissolved in 10 l of isotonic NaCl solution, and thesolution was transferred into commercially available spray containerswith a pump mechanism. The solution could be sprayed into the mouth ornose. One spray shot (about 0.1 ml) corresponded to a dose of about 0.14mg.

Example B04: Protein Binding in Mice Plasma Using Rapid EquilibriumDialysis Materials

-   -   CD1 Mice Plasma: pooled male, K2-EDTA (MSEPLEDTA2,        Bioreclammation, USA    -   Phosphate Buffered Saline (1×PBS), pH 7.4, 100 mM (Sigma, Cat        No. P4417)    -   RED inserts (Pierce, Cat No. 9006, 8 kDa MWCO)    -   Sample Analysis: LC-MS/MS

Methods

Preparation of DMSO Stock Solution

From 20 mM DMSO stock solutions of reference and test compounds, 1 mMDMSO intermediate working solutions are prepared. From 1 mM intermediateworking solutions, 100 μM DMSO working solutions are prepared.

Sample Preparation Procedure:

Selected plasma is brought from −20° C. to 37° C. using water bathbefore its use. Test solution is prepared by adding the DMSO workingsolution of the reference or test compound (2 μL; 100 μM) to theselected plasma (198 μL). Spiked plasma (200 μl) is transferred tosample compartment of RED insert placed in the teflon plate. 350 μl of1×PBS is added in the buffer compartment of RED insert. The teflon plateis covered with sealing mat and agitated at 37° C. for 5 hours at 500RPM in a Thermomixer. After incubation time, an aliquot of plasma (50μl) from sample compartment is mixed with blank 1×PBS (50 μl).Similarly, an aliquot of buffer (50 μl) from buffer compartment is mixedwith blank plasma (50 μl). Quenching solution (200 μL, acetonitrilecontaining internal standard tolbutamide (0.5 μg/mL)) is added and theresulting solutions are mixed using a vortex mixer and centrifuged(Eppendorf 5415, 13792 g). Supernatants are analyzed using a MassSpectrometer. The sample (supernatant fraction, 5 μL) is injected intothe LC-MS/MS instrument.

Chromatographic Conditions:

-   LC-MS/MS: API 4000 LC-MS/MS-   Software: Analyst Version 1.6.1-   Column Phenomenex Synergy 30*4.6*5μ-   Column Oven: 40° C.-   Mode: ESI Positive-   Injection volume: 5 μl-   Flow Rate: 1000 μL/mL-   Buffer: 0.1% Formic acid in Water-   Method: Isocratic Method/Gradient-   Composition: A) 0.1% Formic acid in Water    -   B) 0.1% Formic acid in Methanol

Time Flow Mobile Mobile (Sec) (μL) Phase A Phase B 0.01 1000 10 90 0.41000 10 90 0.8 1000 90 10 1.5 1000 90 10 1.8 1000 10 90 2.5 1000 10 90

Results Calculation

After the concentration of free drug and total drug has been determinedby LCMS/MS, percent plasma protein binding can be calculated as follows:

${\%{fraction}{unbound}} = {\frac{{Drug}{concentration}{in}{buffer}{after}5{hours}}{{Drug}{concentration}{in}{plasma}{after}5{hours}} \times 100}$

Following this protocol, % fraction unbound in plasma from differentspecies can be also measured.

Example B05: Determination of In Vitro Intrinsic Clearance (Cl_(int)-InVitro) with Mouse, Rat and Human Liver Microsomes

In this assay, test compounds are incubated with liver microsomes frommouse, rat and human, and rate of disappearance of drug is determinedusing LC-MS/MS. Conditions used in the assay are summarized below:

Materials

-   -   CD-1 Mice liver microsomes, pooled male (Life Technologies, Cat        No. MSMC-PL) (20 mg/ml)    -   SD Rat liver microsomes, pooled male (Life Technologies, Cat No.        RTMCL-PL) (20 mg/ml)    -   Human liver microsomes, pooled mixed gender (Life Technologies,        Cat No. HMMC-PL) (20 mg/ml)    -   NADPH (SRL Mumbai, Cat No. 99197)    -   Verapamil (Sigma, Cat No. V4629)    -   Atenolol (Sigma, Cat No. A7655)    -   Tolbutamide (Sigma Cat. No. T0891)    -   Assay buffer: 50 mM potassium phosphate buffer, pH 7.4    -   Test & reference compounds: DMSO stock solutions (10 mM        concentration) are prepared and stored at room temperature. An        intermediate 1 mM solution of test or reference compounds is        prepared by mixing 10 μL of 10 mM DMSO stock with 90 μL of DMSO.        The contents are mixed vigorously in a vortex mixer.

Methods

Preparation of Working Solutions of Test and Reference Compounds:

Working solution (100 μM concentration) is prepared by mixing 10 μL of 1mM DMSO solution of test or reference compounds with 90 μL of assaybuffer. The mixture is mixed vigorously in a vortex mixer. Thisresulting solution is containing 10% of DMSO. For the metabolicstability assay, 10 μL of this 100 μM working solution is added to afinal assay volume of 1 mL, yielding final test concentration of 1 μMand DMSO concentration of 0.1%.

Metabolic Stability Assay

Metabolic stability assay is done in a final volume of 1 ml in 50 mMassay buffer, potassium phosphate buffer, pH 7.4. Assay is carried outin duplicates (n=2). A mixture containing 955 μL of assay buffer, 25 μLof liver microsomes and 10 μL of 100 μM test compound solution ispre-incubated for 10 minutes in a water-bath maintained at 37° C. Afterpre-incubation, reaction is started by adding 10 μL of 100 mM NADPHsolution. The solution is mixed and incubated at 37° C. in a water-bath.The final concentration of the different components in the assay is:DMSO 0.1%, test compound 1 μM, liver microsome protein 0.5 mg/ml andNADPH 1 mM.

Aliquots (100 μL) are taken at various time-points (0, 5, 15, 30 and 45minutes) and quenched with 100 μL of acetonitrile containing tolbutamide(500 ng/mL) as internal standard. Samples are mixed using a vortex mixerand centrifuged at 4000 rpm for 10 minutes (Eppendorf 5810R, 3000 g).The supernatants (5 μL) are transferred to 96 well plates and submittedfor LC-MS/MS analysis.

Separate incubations in the same assay mixture, but in the absence ofNADPH, are run in parallel as control for compound stability. Thiscontrol assay is carried out in duplicates (n=2). After pre-incubation,addition of NADPH is omitted and replaced with 10 μL of assay buffer.The final assay volume is 1 mL and aliquots (100 μL) are withdrawn andprocessed for analysis as described for metabolic stability assay.

LC-MS/MS Conditions (Generic Method)

-   LC-MS/MS: API Sciex 4000 with Nexera™ UHPLC-   Software: Analyst Version 1.6.1-   Column: Phenomenex kinetex C18 50×3.0 mm, 2.6μ-   Column Oven: 40° C.-   Mode: ESI Positive-   Injection volume: 5 μl-   Flow Rate: 1000 μL/mL-   Buffer: 0.1% Formic acid in Water-   Method: Isocratic Method/Gradient-   Composition: A) 0.1% Formic acid in Water    -   B) 0.1% Formic acid in Methanol

Time Flow Mobile Mobile (Sec) (μL) Phase A Phase B 0.01 1000 10 90 0.41000 10 90 1 1000 90 10 1.5 1000 90 10 1.8 1000 10 90 3 1000 10 90

Results Calculation

From LC-MS/MS data, amount of drug remaining at different time pointswas determined (% PCR). The logarithm of % PCR was plotted against timeto get the slope value. From the slope value, in vitro T_(1/2) wasdetermined. In vitro intrinsic clearance (Cl_(int)) was calculated usingthe following formulae:

${CL}_{int} = {\frac{0.693}{{In}{vitro}t_{1/2}} \times \frac{{Volume}{of}{incubation}}{{mg}{of}{microsomal}{protein}}}$${{In}{vitro}t_{1/2}} = \frac{0.693}{K_{el}}$

Where K_(el) is Elimination Constant (slope)

Methods for treating the diseases mentioned in this specification, suchas tauopathy, by administering one or more of the compounds of thepresent invention to a patient in need thereof are also object of thisinvention.

If chemical bonds in the structures above are drawn as follows:

or

.

they indicate a defined preferred, i.e. R or S, stereochemistry at atleast one of the atoms to which they are attached to.

This is exemplified below, wherein the structure

is representing preferably one of the two possible enantiomers,

1. A compound of formula (I′)

Wherein R¹, R² denote each independently a straight chain or branchedalkyl having 1 to 6 carbon atoms, wherein 1 to 5 hydrogen atoms may bereplaced by Hal or OH or one of R¹, R² denotes H, while the otherdenotes a straight chain or branched alkyl having 1 to 6 carbon atoms,wherein 1 to 5 hydrogen atoms may be replaced by Hal or OH or R¹ and R²may both denote H, if A denotes the following group:

Z denotes H, OR³, OCF₃, Hal, a straight chain or branched alkyl having 1to 6 carbon atoms, wherein 1 to 5 hydrogen atoms may be replaced by Halor OR³ T¹, T², T³, T⁴ denote each independently CR′″ or N; L is a singlebond or one of the following groups: O, NR^(3′), CH₂, OCH₂, CH₂CH₂,CONR^(3′), CONR^(3′)CH₂, NR³CO, NR³COCH₂, SO₂NR^(3′), NR³SO₂,CONR^(3′)CH₂, CH₂CONR^(3′) SO₂NR^(3′)CH₂, CH₂SO₂NR^(3′), CH₂NR^(3′)CO,NR^(3′)SO₂CH₂, CH₂NR^(3′)SO₂, CH₂O, S(O)(NR^(3′)), N(SO)R^(3′),

m, n denote 0, 1 or 2, wherein m+n is 2; A denotes one of the followinggroups:

X is N or CR′″; X^(a) is N, NR³, C or CR′″; X^(b) is N or C; Y is O, S,SO or SO₂; R′, R″ denote each independently H, Hal or straight chain orbranched alkyl having 1 to 12 carbon atoms; R′″, R′″ independentlydenote H, Hal, NR³R⁴, CHR³R⁴, OR³, CN or a straight chain or branchedalkyl having 1 to 12 carbon atoms, wherein 1 to 3 CH₂-groups may bereplaced by a group selected from O, NR³, S, SO, SO₂, S(O)(NR^(3′)),N(SO)R^(3′), CO, COO, OCO, CONR³, NR³CO,

and wherein 1 to 5 hydrogen atoms may be replaced by Hal, NR³R⁴ or NO₂or by one of the following groups:

or R′″, R″″ independently denote one of the following groups:

R³, R⁴ denote each independently H or a straight chain or branched alkylgroup having 1 to 12 carbon atoms; R^(3a) denote a straight chain orbranched alkyl group having 1 to 12 carbon atoms; W denotes Q or R Qdenotes one of the following groups:

Z¹ is S, O, NR³; Z², Z³ independently denote CR⁵, CR⁶ or N; Z⁴ is N, CH,CON, COCH; Z⁵ is O, NR⁸, CHR⁵, SO₂, S(O)(NR³), N(SO)R^(3′),

Z⁶ is CH₂, CO, S(O)(NR^(3′)), N(SO)R^(3′),

Z⁷ is C(R^(3′))₂, S, O, NR^(3′); s denotes 0 or 1; T is N, CH or CR⁷;R^(3′) denotes H or a straight chain or branched alkyl group having 1 to12 carbon atoms, wherein 1 to 3 CH₂-groups may be replaced by a groupselected from SO₂, CO, 0 and wherein 1 to 5 hydrogen atoms may bereplaced by Hal; R, R⁵, R⁶, R⁷ independently denote H, Hal, CN, OH,NR³R⁴, NO₂ or a straight chain or branched alkyl having 1 to 12 carbonatoms, wherein 1 to 3 CH₂-groups may be replaced by a group selectedfrom O, NR³, S, SO, SO₂, S(O)(NR^(3′)), N(SO)R^(3′), CO, COO, OCO,CONR³, NR³CO

and wherein 1 to 5 hydrogen atoms may be replaced by Hal, NR³R⁴, NO₂,OR³, Het, Ar, Cyc or by one of the following groups:

or R, R⁵, R⁶, R⁷ denote Ar, Het or Cyc or one of the following groups:

R⁸ denotes H or straight chain or branched alkyl having 1 to 12 carbonatoms, wherein 1 to 3 CH₂-groups may be replaced by a group selectedfrom SO, SO₂, S(O)(NR^(3′)), N(SO)R^(3′), CO, COO, OCO, CONR³, NR³CO,and

and further wherein 1 to 5 hydrogen atoms may be replaced by CN, OR³,SR³, Hal, NR³R⁴, NO₂ or by one of the following groups:

or R⁸ denote one of the following groups:

Hal denotes F, Cl, Br or I; Het denotes a saturated, unsaturated oraromatic ring, being monocyclic or bicyclic or fusedbicyclic and having3 to 8 members and containing 1 to 4 heteroatoms selected from N, O andS, which may be substituted by 1 to 3 substituents selected from R⁵, Haland OR³; Ar denotes a 6-membered carbocyclic aromatic ring or a fused ornon-fused bicylic aromatic ring system, which is optionally substitutedby 1 to 3 substituents independently selected from R⁵, OR³ and Hal; Cycdenotes a saturated or an unsaturated carbocyclic ring having from 3 to8 carbon atoms which is optionally substituted by 1 to 3 substituentsindependently selected from R⁵, Hal and OH; t and q denote independentlyfrom one another 0, 1, 2 or 3, with t+q≥1, and pharmaceutically usablederivatives, solvates, salts, prodrugs, tautomers, enantiomers,racemates and stereoisomers thereof, including mixtures thereof in allratios and compounds of formula I, wherein one or more H atoms may bereplaced by D (deuterium).
 2. A compound chosen from the group offormulae Ia, Ib, Ic, Id, Ie, If, Ig and Ih:

wherein A, W, L, T¹, T², T³, T⁴, R′″, m and n have the meaning given inclaim 1 and wherein R¹ and R² denote each independently a straight chainor branched alkyl having 1 to 6 carbon atoms, wherein 1 to 5 hydrogenatoms may be replaced by Hal or OH.
 3. A mixture comprising compounds offormulae Ia and Ic or a mixture comprising compounds of formulae Ib andId or a mixture comprising compounds of formulae Ie and If or a mixturecomprising compounds of formulae Ig and Ih according to claim 2, havingidentical groups A, W, L, R¹, R², T¹, T², T³, T⁴, R′″, m and n, in equalor unequal amounts.
 4. A compound of formula I according to any one ofclaims 1 to 3, wherein R¹ is methyl and R² denotes H or wherein R¹ andR² are both methyl.
 5. A compound of formula I according to any one ofclaims 1 to 4, wherein A denotes one of the following groups:

wherein R³, X, R′, R″ and R′″ have the meaning given in claim
 1. 6. Acompound of formula I according to any one of claims 1 to 5, wherein thegroup Q denotes H or one of the following groups:

wherein X, R′″, R³, T, Z⁵, Z⁶, R⁶ and R⁷ have the meaning given inclaim
 1. 7. A compound of formula I according to any one of claims 1 to6, wherein R, R⁵, R⁶, R⁷ are independently selected from H, ON, SO₂CH₃,SO₂CH₂CH₃, SO₂CH₂CH₂OH, SO₂CH₂CH₂OCH₃, S(O)(NR^(3′))CH₃,S(O)(NR^(3′))CH₂CH₃, S(O)(NR^(3′))CH₂CH₂OH, S(O)(NR^(3′))CH₂CH₂OCH₃,N(SO)R^(3′)CH₃, N(SO)R^(3′)CH₂CH₃, N(SO)R^(3′)CH₂CH₂OH,N(SO)R^(3′)CH₂CH₂OCH₃, Hal, NR³R⁴, NO₂, phenyl, benzyl, CH₂-pyridyl,O-phenyl, O-pyridyl, O-pyrimidinyl, O-benzyl, 2-, 3- or 4-hydroxy ormethoxyphenyl, alkyl, alkoxy (Oalkyl), hydroxyalkylen, alkoxyalkylen,COOH, COOalkyl, CONHalkyl, CONH₂, CON(CH₃)₂, NHCOalkyl, NHCOCH₃,NHCOphenyl, NHCOpyridyl, NHCH₂CH₃, NHCH₂CH₂CH₃, NHCOCH₂CH₂OH,CO—N-morpholinyl, CON(CH₃)CH₂CH₂N(CH₃)₂, CO-1-piperidinyl,CO-4-hydroxy-1-piperidinyl, CO-1-piperazinyl, CO-4-methyl-1-piperazinyl,CH₂—N-morpholinyl, CH₂N(H)COCH₃, CH₂N(CH₃)COCH₃, CH₂NH₂, NH₂, CH(OH)CH₃,CH(OR³)CH₃ and a group

wherein t+q is 2 or 3, and Z⁷, R^(3′), R³ and R⁴ have the meaning givenin claim
 1. 8. A compound of formula I according to any one of claims 1to 7, wherein L is a single bond or —O—.
 9. A compound of formula Iaccording to any one of claims 1 to 8, wherein m and n simultaneouslydenote
 1. 10. A compound according to claim 1, selected from thefollowing group: No Structure 1

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and/or and pharmaceutically usable derivatives, solvates, salts,tautomers, enantiomers, racemates and stereoisomers thereof, includingmixtures thereof in all ratios.
 11. A compound of formula (I′) accordingto any one of claims 1 to 10 for use as a medicament.
 12. A compound offormula (I′) according to any one of claims 1 to 10 and pharmaceuticallyusable derivatives, solvates, salts, tautomers, enantiomers, racematesand stereoisomers thereof, including mixtures thereof in all ratios, foruse in a method of treating a condition selected from the groupconsisting of neurodegenerative diseases, diabetes, cancer,cardiovascular diseases and stroke.
 13. A compound for use in atreatment of a condition according to claim 12, wherein the condition isselected from the group of one or more tauopathies and Alzheimer'sdisease, Dementia, Amyotrophic lateral sclerosis (ALS), Amyotrophiclateral sclerosis with cognitive impairment (ALSci), Argyrophilic graindisease, Behavioural variant frontotemporal dementia (BvFTD), Bluitdisease, Chronic traumatic encephalopathy, Corticobasal degeneration(CBP), Dementia pugilistica, Diffuse neurofibrillary tangles withcalcification, Down's syndrome, Familial British dementia, FamilialDanish dementia, Frontotemporal dementia with parkinsonism linked tochromosome 17 (FTDP-17), Frontotemporal lobar degeneration (FTLD),Ganglioglioma, Gangliocytoma, Gerstmann-Straussler-Scheinker disease,Globular glia tauopathy, Guadeloupean parkinsonism, Hallevorden-Spatzdisease (neurodegeneration with brain iron accumulation type 1), Leadencephalopathy, Lipofuscinosis, Meningioangiomatosis, Multiple systematrophy, Myotonic dystrophy, Niemann-Pick disease (type C),Pallido-ponto-nigral degeneration, Parkinsonism-dementia complex ofGuam, Pick's disease (PiD), Parkinson's disease dementia,Postencephalitic parkinsonism (PEP), Primary progressive aphasia, Priondiseases (including Creutzfeldt-Jakob Disease (CJD), Progressivenonfluent aphasia, Variant Creutzfeldt-Jakob Disease (vCJD)), FatalFamilial Insomnia, Kuru, Progressive supercortical gliosis, Progressivesupranuclear palsy (PSP), Semantic dementia, Steele-Richardson-Olszewskisyndrome, Subacute sclerosing panencephalitis, Tangle-only dementia,Tuberous sclerosis, Huntington's disease and Parkinson's disease,preferably one or more tauopathies and Alzheimer's disease.
 14. A methodfor treating a tauopathy, wherein a compound defined in any one ofclaims 1 to 10 is administered to a mammal in need of such treatment.15. A method for inhibiting a glycosidase, wherein a system expressingthe glycosidase is contacted with a compound as defined in any one ofclaims 1 to 10 under in-vitro conditions such that the glycosidase isinhibited.
 16. A pharmaceutical composition comprising as activeingredient a compound according to any one of claims 1 to 10 togetherwith pharmaceutically tolerable adjuvants and/or excipients, optionallyin combination with one or more further active ingredients.